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Previous release (v1)
2024-05-02 16:27:10, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_033515 4414 bp mRNA linear PRI 17-JUL-2023
DEFINITION Homo sapiens Rho GTPase activating protein 18 (ARHGAP18), mRNA.
ACCESSION NM_033515
VERSION NM_033515.3
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 4414)
AUTHORS Dibus M, Brabek J and Rosel D.
TITLE A Screen for PKN3 Substrates Reveals an Activating Phosphorylation
of ARHGAP18
JOURNAL Int J Mol Sci 21 (20), 7769 (2020)
PUBMED 33092266
REMARK GeneRIF: A Screen for PKN3 Substrates Reveals an Activating
Phosphorylation of ARHGAP18.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 4414)
AUTHORS Coleman PR, Lay AJ, Ting KK, Zhao Y, Li J, Jarrah S, Vadas MA and
Gamble JR.
TITLE YAP and the RhoC regulator ARHGAP18, are required to mediate
flow-dependent endothelial cell alignment
JOURNAL Cell Commun Signal 18 (1), 18 (2020)
PUBMED 32013974
REMARK GeneRIF: YAP and the RhoC regulator ARHGAP18, are required to
mediate flow-dependent endothelial cell alignment.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 4414)
AUTHORS Jomoui W, Tepakhan W, Yamsri S, Srivorakun H, Fucharoen G and
Fucharoen S.
TITLE A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is
associated with the expression of Hb F in hemoglobin E-related
disorders
JOURNAL Ann Hematol 99 (1), 23-29 (2020)
PUBMED 31776727
REMARK GeneRIF: novel SNP rs11759328 on Rho GTPase-activating protein 18
gene is associated with the expression of Hb F in hemoglobin
E-related disorders.
REFERENCE 4 (bases 1 to 4414)
AUTHORS Chen J, Huang X, Wang W, Xie H, Li J, Hu Z, Zheng Z, Li H and Teng
L.
TITLE LncRNA CDKN2BAS predicts poor prognosis in patients with
hepatocellular carcinoma and promotes metastasis via the
miR-153-5p/ARHGAP18 signaling axis
JOURNAL Aging (Albany NY) 10 (11), 3371-3381 (2018)
PUBMED 30510148
REMARK GeneRIF: This study revealed that lncRNA CDKN2BAS promotes HCC
metastasis by regulating the miR-153-5p/ARHGAP18 signaling.
REFERENCE 5 (bases 1 to 4414)
AUTHORS He Y, Luo J, Chen Y, Zhou X, Yu S, Jin L, Xiao X, Jia S and Liu Q.
TITLE ARHGAP18 is a novel gene under positive natural selection that
influences HbF levels in beta-thalassaemia
JOURNAL Mol Genet Genomics 293 (1), 207-216 (2018)
PUBMED 28983712
REMARK GeneRIF: Our data suggest that ARHGAP18, which was located by the
SNP rs11759328 via positive selection, plays a potential role in
regulating HbF expression in beta-thalassaemia and may be a
promising therapeutic target
REFERENCE 6 (bases 1 to 4414)
AUTHORS Cronin S, Tomik B, Bradley DG, Slowik A and Hardiman O.
TITLE Screening for replication of genome-wide SNP associations in
sporadic ALS
JOURNAL Eur J Hum Genet 17 (2), 213-218 (2009)
PUBMED 18987618
REMARK GeneRIF: Observational study and genome-wide association study of
gene-disease association. (HuGE Navigator)
REFERENCE 7 (bases 1 to 4414)
AUTHORS Li X, Liu Q, Liu S, Zhang J and Zhang Y.
TITLE New member of the guanosine triphosphatase activating protein
family in the human epididymis
JOURNAL Acta Biochim Biophys Sin (Shanghai) 40 (10), 855-863 (2008)
PUBMED 18850050
REFERENCE 8 (bases 1 to 4414)
AUTHORS Wang AG, Yoon SY, Oh JH, Jeon YJ, Kim M, Kim JM, Byun SS, Yang JO,
Kim JH, Kim DG, Yeom YI, Yoo HS, Kim YS and Kim NS.
TITLE Identification of intrahepatic cholangiocarcinoma related genes by
comparison with normal liver tissues using expressed sequence tags
JOURNAL Biochem Biophys Res Commun 345 (3), 1022-1032 (2006)
PUBMED 16712791
REFERENCE 9 (bases 1 to 4414)
AUTHORS Lehner B and Sanderson CM.
TITLE A protein interaction framework for human mRNA degradation
JOURNAL Genome Res 14 (7), 1315-1323 (2004)
PUBMED 15231747
REFERENCE 10 (bases 1 to 4414)
AUTHORS Mungall AJ, Palmer SA, Sims SK, Edwards CA, Ashurst JL, Wilming L,
Jones MC, Horton R, Hunt SE, Scott CE, Gilbert JG, Clamp ME, Bethel
G, Milne S, Ainscough R, Almeida JP, Ambrose KD, Andrews TD,
Ashwell RI, Babbage AK, Bagguley CL, Bailey J, Banerjee R, Barker
DJ, Barlow KF, Bates K, Beare DM, Beasley H, Beasley O, Bird CP,
Blakey S, Bray-Allen S, Brook J, Brown AJ, Brown JY, Burford DC,
Burrill W, Burton J, Carder C, Carter NP, Chapman JC, Clark SY,
Clark G, Clee CM, Clegg S, Cobley V, Collier RE, Collins JE, Colman
LK, Corby NR, Coville GJ, Culley KM, Dhami P, Davies J, Dunn M,
Earthrowl ME, Ellington AE, Evans KA, Faulkner L, Francis MD,
Frankish A, Frankland J, French L, Garner P, Garnett J, Ghori MJ,
Gilby LM, Gillson CJ, Glithero RJ, Grafham DV, Grant M, Gribble S,
Griffiths C, Griffiths M, Hall R, Halls KS, Hammond S, Harley JL,
Hart EA, Heath PD, Heathcott R, Holmes SJ, Howden PJ, Howe KL,
Howell GR, Huckle E, Humphray SJ, Humphries MD, Hunt AR, Johnson
CM, Joy AA, Kay M, Keenan SJ, Kimberley AM, King A, Laird GK,
Langford C, Lawlor S, Leongamornlert DA, Leversha M, Lloyd CR,
Lloyd DM, Loveland JE, Lovell J, Martin S, Mashreghi-Mohammadi M,
Maslen GL, Matthews L, McCann OT, McLaren SJ, McLay K, McMurray A,
Moore MJ, Mullikin JC, Niblett D, Nickerson T, Novik KL, Oliver K,
Overton-Larty EK, Parker A, Patel R, Pearce AV, Peck AI, Phillimore
B, Phillips S, Plumb RW, Porter KM, Ramsey Y, Ranby SA, Rice CM,
Ross MT, Searle SM, Sehra HK, Sheridan E, Skuce CD, Smith S, Smith
M, Spraggon L, Squares SL, Steward CA, Sycamore N, Tamlyn-Hall G,
Tester J, Theaker AJ, Thomas DW, Thorpe A, Tracey A, Tromans A,
Tubby B, Wall M, Wallis JM, West AP, White SS, Whitehead SL,
Whittaker H, Wild A, Willey DJ, Wilmer TE, Wood JM, Wray PW, Wyatt
JC, Young L, Younger RM, Bentley DR, Coulson A, Durbin R, Hubbard
T, Sulston JE, Dunham I, Rogers J and Beck S.
TITLE The DNA sequence and analysis of human chromosome 6
JOURNAL Nature 425 (6960), 805-811 (2003)
PUBMED 14574404
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
CB149638.1, BM557223.1, AB053293.1 and AL450310.18.
On Nov 22, 2018 this sequence version replaced NM_033515.2.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: SRR1660803.158316.1,
SRR1803614.93837.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000368149.3/ ENSP00000357131.2
RefSeq Select criteria :: based on single protein-coding transcript
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-107 CB149638.1 49-155
108-786 BM557223.1 93-771
787-3451 AB053293.1 633-3297
3452-4414 AL450310.18 30892-31854 c
FEATURES Location/Qualifiers
source 1..4414
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6q22.33"
gene 1..4414
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Rho GTPase activating protein 18"
/db_xref="GeneID:93663"
/db_xref="HGNC:HGNC:21035"
/db_xref="MIM:613351"
exon 1..154
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:369292520"
variation 3
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1211131296"
variation 4..8
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:1230315967"
variation 4
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774886940"
variation 5
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375985630"
variation 7
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:764895871"
variation 9
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774886723"
variation 11
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329859035"
variation 15
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751204070"
variation 16
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:572164177"
variation 18..23
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="agaaag"
/replace="agaaagaaag"
/db_xref="dbSNP:1228063183"
variation 18
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:760545668"
variation 20
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767787696"
variation 22
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1429719918"
variation 23
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:759621070"
variation 25
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1774885912"
variation 26
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774621306"
variation 28
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584128679"
variation 29
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:771066780"
variation 30
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:185923246"
variation 31
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:773730661"
variation 32
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774885443"
variation 34
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422545194"
variation 36
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:765968468"
variation 38
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114564361"
variation 40
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182825122"
variation 41
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:770245203"
CDS 42..2033
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="rho-type GTPase-activating protein 18"
/codon_start=1
/product="rho GTPase-activating protein 18"
/protein_id="NP_277050.2"
/db_xref="CCDS:CCDS34535.1"
/db_xref="GeneID:93663"
/db_xref="HGNC:HGNC:21035"
/db_xref="MIM:613351"
/translation="
MSWLSSSQGVVLTAYHPSGKDQTVGNSHAKAGEEATSSRRYGQYTMNQESTTIKVMEKPPFDRSISQDSLDELSMEDYWIELENIKKSSENSQEDQEVVVVKEPDEGELEEEWLKEAGLSNLFGESAGDPQESIVFLSTLTRTQAAAVQKRVETVSQTLRKKNKQYQIPDVRDIFAQQRESKETAPGGTESQSLRTNENKYQGRDDEASNLVGEEKLIPPEETPAPETDINLEVSFAEQALNQKESSKEKIQKSKGDDATLPSFRLPKDKTGTTRIGDLAPQDMKKVCHLALIELTALYDVLGIELKQQKAVKIKTKDSGLFCVPLTALLEQDQRKVPGMRIPLIFQKLISRIEERGLETEGLLRIPGAAIRIKNLCQELEAKFYEGTFNWESVKQHDAASLLKLFIRELPQPLLSVEYLKAFQAVQNLPTKKQQLQALNLLVILLPDANRDTLKALLEFLQRVIDNKEKNKMTVMNVAMVMAPNLFMCHALGLKSSEQREFVMAAGTANTMHLLIKYQKLLWTIPKFIVNQVRKQNTENHKKDKRAMKKLLKKMAYDREKYEKQDKSTNDADVPQGVIRVQAPHLSKVSMAIQLTEELKASDVLARFLSQESGVAQTLKKGEVFLYEIGGNIGERCLDDDTYMKDLYQLNPNAEWVIKSKPL"
misc_feature 84..152
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="propagated from UniProtKB/Swiss-Prot (Q8N392.3);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 237..239
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q8K0Q5; propagated from
UniProtKB/Swiss-Prot (Q8N392.3); phosphorylation site"
misc_feature 246..248
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q8K0Q5; propagated from
UniProtKB/Swiss-Prot (Q8N392.3); phosphorylation site"
misc_feature 513..515
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Phosphothreonine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q8N392.3); phosphorylation site"
misc_feature 576..722
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="propagated from UniProtKB/Swiss-Prot (Q8N392.3);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 768..872
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="propagated from UniProtKB/Swiss-Prot (Q8N392.3);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 828..830
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q8N392.3); phosphorylation site"
misc_feature 1002..1643
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="RhoGAP (GTPase-activator protein [GAP] for Rho-like
small GTPases) domain of ArhGAP18-like proteins. The
function of ArhGAP18 is unknown. Small GTPases cluster
into distinct families, and all act as molecular switches,
active in their GTP-bound form but...; Region:
RhoGAP_ARHGAP18; cd04391"
/db_xref="CDD:239856"
misc_feature order(1134..1136,1251..1253,1263..1265,1470..1472,
1479..1484,1566..1568)
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="putative GTPase interaction site [polypeptide
binding]; other site"
/db_xref="CDD:239856"
misc_feature 1134..1136
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="catalytic residue [active]"
/db_xref="CDD:239856"
misc_feature 1869..1871
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q8N392.3); phosphorylation site"
variation 47
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246425933"
variation 51
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774885059"
variation 53
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210816357"
variation 54
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465445945"
variation 55
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:748549945"
variation 57
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:143944879"
variation 58
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774884643"
variation 65
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:755354145"
variation 66
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:745571458"
variation 67
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778674538"
variation 72
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1362685336"
variation 74
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114564321"
variation 75
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:756872004"
variation 76
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486022407"
variation 77
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:958226927"
variation 78
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:753354837"
variation 81
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:868593122"
variation 84
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393143118"
variation 85
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1291314665"
variation 86
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774883698"
variation 87
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:764162238"
variation 88
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584128612"
variation 89
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1190063079"
variation 90
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352133872"
variation 91
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:762625490"
variation 92
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187941489"
variation 94
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1774883205"
variation 95
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767275285"
variation 96
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388692124"
variation 97
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430671152"
variation 99
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774882674"
variation 104
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:138062778"
variation 105
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1450292189"
variation 108
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3752536"
variation 109
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766566421"
variation 110
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292977362"
variation 111
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489473472"
variation 112
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140129403"
variation 114
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373799018"
variation 115
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:996213202"
variation 117
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1774880440"
variation 118
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:773208947"
variation 122
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:201122002"
variation 123
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774880243"
variation 125
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056478435"
variation 126
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276491093"
variation 127
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748659488"
variation 131
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330169195"
variation 132
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368260912"
variation 133
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114564190"
variation 135..138
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1774879625"
variation 135
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:34390841"
variation 136..144
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gggaggaag"
/replace="gggaggaagggaggaag"
/db_xref="dbSNP:762523570"
variation 136
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1317069414"
variation 137
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037819420"
variation 147
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1774879523"
variation 148
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1774879459"
variation 151
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:570477591"
variation 152
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374586820"
exon 155..357
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 156
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:202226965"
variation 157
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143012976"
variation 158
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:149116232"
variation 161
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:769229671"
variation 162
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378325155"
variation 164
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1158544953"
variation 165
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:747673241"
variation 166
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368392829"
variation 168
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773477665"
variation 170
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754877067"
variation 174
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1183021815"
variation 175
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1441687953"
variation 178
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:188042743"
variation 183
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773477288"
variation 189
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1201863203"
variation 190
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1562707004"
variation 191
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483390948"
variation 192
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267045195"
variation 193
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:779881431"
variation 195
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261573607"
variation 197
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773476752"
variation 199
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114500076"
variation 202
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:758183088"
variation 204
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025875419"
variation 208
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:750681949"
variation 209
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240379261"
variation 210
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340286070"
variation 214
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391042186"
variation 215
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761817778"
variation 216
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773476251"
variation 219
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:753911423"
variation 221
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584080793"
variation 228
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:779596981"
variation 229
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757913140"
variation 232
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272980209"
variation 234
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773475854"
variation 238
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:772632806"
variation 239
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:759949551"
variation 241
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288226913"
variation 243
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:367817344"
variation 244
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:970677390"
variation 245
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:924145915"
variation 247
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773473525"
variation 251
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:772789486"
variation 253
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773473387"
variation 258
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562706905"
variation 260
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769439947"
variation 263
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442719396"
variation 264
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200222519"
variation 265
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360464157"
variation 270
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:146502081"
variation 271
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1465914159"
variation 273
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754273630"
variation 274
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773472691"
variation 275
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:768036176"
variation 278
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747015023"
variation 282
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773472469"
variation 285
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231671987"
variation 292
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:764613446"
variation 293
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773472237"
variation 294
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302949146"
variation 296
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779932719"
variation 304
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:758236154"
variation 308
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247466475"
variation 312
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021414603"
variation 313
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:11544371"
variation 314
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773471829"
variation 317
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214375163"
variation 319
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562706809"
variation 321
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1260686659"
variation 326
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773471536"
variation 327
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:745609774"
variation 328
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297229306"
variation 329..332
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:773382444"
variation 329
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1432075779"
variation 330
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773471273"
variation 332
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779031349"
variation 333
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777450768"
variation 334
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:200011410"
variation 335
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390987922"
variation 339
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:144120797"
variation 341
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249080238"
variation 344
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:373679715"
variation 345
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:140336106"
variation 351
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773470552"
variation 354
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753298352"
exon 358..593
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 362
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1010764081"
variation 367
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:898608856"
variation 368
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:756993026"
variation 369
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:749594026"
variation 371
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:777830329"
variation 373
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:756313707"
variation 379
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1738652343"
variation 380
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773383618"
variation 390
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375107476"
variation 392
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:768170205"
variation 393
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353126704"
variation 395
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584077233"
variation 398
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114496627"
variation 403
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:532064655"
variation 404
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773383121"
variation 407
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1405576064"
variation 410
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146587551"
variation 411
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:150003221"
variation 412
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773382739"
variation 415
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411497322"
variation 417
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:200033041"
variation 422
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1174966525"
variation 426
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:139290398"
variation 428
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:760205913"
variation 429
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773382282"
variation 431
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176564466"
variation 433
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:150828400"
variation 434
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:772015050"
variation 437
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:759579799"
variation 439
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:565512996"
variation 443
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773381880"
variation 449
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773381799"
variation 450
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:770802381"
variation 452
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:774917496"
variation 454
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773381572"
variation 456
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:749015404"
variation 464
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051482752"
variation 465
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:371036479"
variation 466
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:770101592"
variation 470
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584077134"
variation 491
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280946288"
variation 492
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:922082718"
variation 493
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773380990"
variation 494
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474756269"
variation 499
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1328564156"
variation 500
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:540465556"
variation 502
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:377629902"
variation 503
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:34022250"
variation 508
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:752146514"
variation 512..522
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ga"
/replace="gaccttgagga"
/db_xref="dbSNP:769082558"
variation 514
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1445490841"
variation 515
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773379889"
variation 518
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:780402227"
variation 521
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:758810786"
variation 522..529
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:749346165"
variation 522
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336339504"
variation 523
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:984120103"
variation 524
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773379446"
variation 525
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456302238"
variation 527..535
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaca"
/replace="aaacaaaca"
/db_xref="dbSNP:1421372017"
variation 529
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773378995"
variation 530
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1562704815"
variation 531..533
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1773378681"
variation 531
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430061532"
variation 532
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:750711613"
variation 533
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157638779"
variation 536
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:11544372"
variation 538
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773378415"
variation 547..554
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="ctgacgtc"
/db_xref="dbSNP:1773378109"
variation 547
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:763736215"
variation 551
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181668271"
variation 552
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:375316938"
variation 559
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:34340880"
variation 560
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:767085630"
variation 561
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464535323"
variation 563..572
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="atttgctcaa"
/db_xref="dbSNP:780128183"
variation 565
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321074471"
variation 569
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:369628546"
variation 570
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201824460"
variation 572
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217982305"
variation 574
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773377087"
variation 575
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773377026"
variation 577
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:960031297"
variation 578
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1773376906"
variation 580
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562704762"
variation 584
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:540086198"
variation 585
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:774399070"
variation 587
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773376610"
variation 588
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:969461309"
variation 589
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584076936"
variation 591
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226412945"
variation 592
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773376290"
exon 594..657
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 594
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773279475"
variation 595
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:780639831"
variation 597
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773279234"
variation 598
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:565909889"
variation 600
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141026635"
variation 602
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427088505"
variation 603
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773278963"
variation 605
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:147325546"
variation 613
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:368664665"
variation 614
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:762618294"
variation 616
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="a"
/db_xref="dbSNP:1483020428"
variation 616
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1437939918"
variation 624
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293503473"
variation 627
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752390148"
variation 632
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:767136952"
variation 633
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773278240"
variation 638
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1773278155"
variation 639
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347775328"
variation 640
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773277996"
variation 641
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773277932"
variation 645
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:144039256"
variation 647
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773277754"
variation 648
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:750995744"
variation 651
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:140069506"
variation 652
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313012533"
variation 654
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388565595"
variation 655
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:762742945"
variation 656
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114492283"
variation 657
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:773277447"
exon 658..827
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 659
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:757825075"
variation 660
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:564963735"
variation 661
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773142431"
variation 662
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773142308"
variation 663
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1160155700"
variation 665
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:767734533"
variation 671
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1380459151"
variation 672
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773142036"
variation 673
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562700720"
variation 674
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1773141904"
variation 682
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562700715"
variation 683
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:759647793"
variation 684
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456981382"
variation 690
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:190006516"
variation 693
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:774349348"
variation 694
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773141492"
variation 695
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1160899685"
variation 698
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:771441084"
variation 699
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253717248"
variation 701
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773141208"
variation 702..707
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gag"
/replace="gaggag"
/replace="gaggaggag"
/db_xref="dbSNP:775477935"
variation 706
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773141148"
variation 707
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114487579"
variation 709
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:763511682"
variation 710
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:144510851"
variation 711
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:149277156"
variation 715
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255661683"
variation 716
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:138425497"
variation 719
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="t"
/db_xref="dbSNP:769872908"
variation 719
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114487553"
variation 723..729
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aca"
/replace="acagaca"
/db_xref="dbSNP:746019513"
variation 728
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:779602809"
variation 729
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199525893"
variation 731
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483409154"
variation 733
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1773140070"
variation 737
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251221930"
variation 738
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454764919"
variation 741
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:778621532"
variation 742
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:756820590"
variation 743
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320015235"
variation 744
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263796006"
variation 746
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:753762415"
variation 752
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:367609881"
variation 753
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:767731622"
variation 759
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:759697034"
variation 761
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:751768603"
variation 762
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185102272"
variation 766
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:558829279"
variation 770
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:375352117"
variation 773..778
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="agag"
/replace="agagag"
/db_xref="dbSNP:1562700595"
variation 774
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238431856"
variation 779
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:773613072"
variation 783
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1055545656"
variation 784
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:34706122"
variation 785..786
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:36088992"
variation 785
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448160931"
variation 786
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287021687"
variation 788
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:776993730"
variation 789..792
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1773137885"
variation 794
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:142347893"
variation 796
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166376468"
variation 799
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1356136872"
variation 800
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:745580689"
variation 803
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778674654"
variation 808
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1773137401"
variation 809
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:770616889"
variation 810
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:370593148"
variation 811
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:777607504"
variation 812
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773137118"
variation 817
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1773137046"
variation 819
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328270716"
variation 825
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:756017180"
exon 828..993
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 828
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:781077876"
variation 832
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:754789237"
variation 834
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:112705608"
variation 835
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746764292"
variation 836
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1388023161"
variation 837
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232644851"
variation 840
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:780258445"
variation 842
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:376985316"
variation 843
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393430789"
variation 844
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:750594073"
variation 852
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273893465"
variation 853
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:145543683"
variation 854
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:150029445"
variation 862
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285183113"
variation 863
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224007683"
variation 864
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:754442961"
variation 865
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1789150272"
variation 867
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:543678244"
variation 868
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1789149906"
variation 869
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:758269589"
variation 870
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461237457"
variation 874
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354769866"
variation 875
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:761155904"
variation 876
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:775933311"
variation 877
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:765965041"
variation 878..880
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="cgc"
/db_xref="dbSNP:2114470299"
variation 878
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:369067311"
variation 879
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:772736255"
variation 886
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:769386921"
variation 888
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1175853139"
variation 889
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1789149005"
variation 891
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1437784797"
variation 893
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747636881"
variation 895
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1789148759"
variation 896
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180262081"
variation 897
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:936879271"
variation 901
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473121139"
variation 903
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1789148462"
variation 905
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:200617893"
variation 907
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:776579064"
variation 908
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:2114470243"
variation 909
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:768513372"
variation 911
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204326686"
variation 912
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:746819538"
variation 915
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1281995363"
variation 917..918
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1373786684"
variation 917
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:562997986"
variation 919
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453471241"
variation 920
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:954969868"
variation 921
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283278656"
variation 926
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1789147523"
variation 929
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449986022"
variation 931
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1789147344"
variation 937
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:140355619"
variation 942
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336856755"
variation 944
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408184704"
variation 949
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:375652253"
variation 950
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114470189"
variation 956
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1345128240"
variation 960
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1371006187"
variation 962
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:778978249"
variation 963
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1402875561"
variation 964
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1789146527"
variation 966
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1789146448"
variation 967
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1789146077"
variation 975
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1409129358"
variation 980
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357011543"
variation 985
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:974780803"
variation 991
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183269222"
exon 994..1085
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 994
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268013869"
variation 998
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1384526176"
variation 1000
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:903298332"
variation 1002
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779229088"
variation 1003..1008
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1292136331"
variation 1003
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1789096957"
variation 1004
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:771213679"
variation 1010
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:569516329"
variation 1011
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:151200685"
variation 1016
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:372951773"
variation 1017
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267531118"
variation 1018
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214603126"
variation 1022
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1789096351"
variation 1023
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341683694"
variation 1024
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:191935343"
variation 1025
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781529755"
variation 1026
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:143111967"
variation 1030
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304034011"
variation 1032
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262239886"
variation 1033
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461693039"
variation 1036
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371514777"
variation 1038
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172631163"
variation 1041
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:751802275"
variation 1045
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:978714652"
variation 1047
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:968717880"
variation 1049
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1789095360"
variation 1051
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:764954361"
variation 1054
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114467468"
variation 1057
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:761511980"
variation 1061
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379041995"
variation 1062
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:753480406"
variation 1063
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:539196958"
variation 1068
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775517266"
variation 1072
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409081537"
variation 1078
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:771866699"
variation 1085
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1789094525"
exon 1086..1163
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1086
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:577421005"
variation 1087
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203907752"
variation 1088
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334345945"
variation 1089
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788982085"
variation 1092
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:774345812"
variation 1093
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1705323021"
variation 1095
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054943841"
variation 1096
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:148956917"
variation 1099
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334823457"
variation 1105
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1690977901"
variation 1106
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114461735"
variation 1107
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114461731"
variation 1108
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:932944238"
variation 1110
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402836422"
variation 1116
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584044910"
variation 1120
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788980951"
variation 1123
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:921412346"
variation 1126
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584044889"
variation 1131
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:762820395"
variation 1133
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:758345227"
variation 1133
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:34725884"
variation 1134
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:543407407"
variation 1135
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788980414"
variation 1138
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584044861"
variation 1139
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748272002"
variation 1140
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:373154529"
variation 1141
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:372455896"
variation 1142
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:187959392"
variation 1145
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="a"
/db_xref="dbSNP:1788979943"
variation 1146
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:768775714"
variation 1149
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788979798"
variation 1151
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:747506599"
variation 1152
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:780513485"
variation 1154
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240814373"
variation 1155
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:758781370"
variation 1160
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461369542"
variation 1161
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777409816"
exon 1164..1323
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1164
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:764976832"
variation 1166
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165654757"
variation 1167
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:866232077"
variation 1171
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1426483011"
variation 1172
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195027952"
variation 1173
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:761641707"
variation 1176
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114457198"
variation 1179
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114457197"
variation 1180
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267241100"
variation 1181
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:34386438"
variation 1182
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243768390"
variation 1184
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475054060"
variation 1185
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:372831811"
variation 1187
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:570444619"
variation 1189
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:775492236"
variation 1190
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051905223"
variation 1195
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1229841224"
variation 1196
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341558931"
variation 1198
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1278808916"
variation 1199
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:772127660"
variation 1201
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:541221915"
variation 1203
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:140706963"
variation 1204..1206
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:770330803"
variation 1204
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:771253438"
variation 1207..1212
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttaatt"
/replace="ttaattaatt"
/db_xref="dbSNP:759642752"
variation 1209
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788889903"
variation 1211
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:749619265"
variation 1213
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:780741805"
variation 1214
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1268740231"
variation 1216
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788889513"
variation 1218
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326427764"
variation 1219
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:768290947"
variation 1220
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746644557"
variation 1221
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:779773986"
variation 1224
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757946610"
variation 1227
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:750430334"
variation 1229
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:778860347"
variation 1231
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757033582"
variation 1232
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788888807"
variation 1233
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:372212567"
variation 1235
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:764232980"
variation 1238
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788888677"
variation 1239
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282969200"
variation 1240
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321692526"
variation 1242
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788888497"
variation 1244
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:760947869"
variation 1245..1250
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ctg"
/replace="ctgctg"
/db_xref="dbSNP:988974839"
variation 1249
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1788888338"
variation 1256
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:752913481"
variation 1257
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:921449099"
variation 1259
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370262467"
variation 1260
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788887951"
variation 1263
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759590664"
variation 1264
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200791539"
variation 1268
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788887640"
variation 1269
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:555610763"
variation 1275
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:763234355"
variation 1277..1283
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gccactg"
/replace="gccactggccactg"
/db_xref="dbSNP:776598106"
variation 1280
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:773570626"
variation 1284
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788887228"
variation 1286
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277449352"
variation 1290
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:770047769"
variation 1292
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:746695909"
variation 1293
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775258000"
variation 1295
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449760186"
variation 1296
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404616977"
variation 1298
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788886742"
variation 1299
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:771726436"
variation 1301
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788886605"
variation 1312
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788886542"
variation 1315
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:745331619"
variation 1316
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407685449"
variation 1317
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157139967"
variation 1319
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778718760"
exon 1324..1406
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1324
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290636352"
variation 1329
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788844615"
variation 1333
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179146587"
variation 1334
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788844460"
variation 1336
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788844391"
variation 1340
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:773967441"
variation 1341
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:770345629"
variation 1343
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:147754877"
variation 1344
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:981586849"
variation 1345
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:202043590"
variation 1349
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166567408"
variation 1353..1355
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="gct"
/db_xref="dbSNP:1788843625"
variation 1353
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:917705561"
variation 1354
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014698939"
variation 1355..1357
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1788843536"
variation 1358
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788843448"
variation 1360
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:777550443"
variation 1361
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:370858739"
variation 1362
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449718197"
variation 1365
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788843080"
variation 1368
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332619208"
variation 1374
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378991448"
variation 1375
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:781400499"
variation 1377
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584039451"
variation 1378
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394663040"
variation 1379
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584039444"
variation 1382
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402317047"
variation 1385
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:755138072"
variation 1393
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788842392"
variation 1395
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:751720325"
variation 1398
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788842214"
variation 1399
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114454588"
variation 1401
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114454586"
variation 1406
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:766518423"
exon 1407..1613
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1410
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1461584315"
variation 1413
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788724100"
variation 1416
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114448714"
variation 1417
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:773168308"
variation 1418
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788723945"
variation 1425
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1172847613"
variation 1426
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418018226"
variation 1429
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182006804"
variation 1431
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:145639226"
variation 1433
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428427211"
variation 1435
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="t"
/db_xref="dbSNP:1471643525"
variation 1436
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788723385"
variation 1437
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:747953706"
variation 1438
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1434670161"
variation 1440
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267694096"
variation 1443
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:781024902"
variation 1447..1453
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1788722948"
variation 1448
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:768406539"
variation 1455
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788722884"
variation 1459
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239487464"
variation 1464
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:747301742"
variation 1467
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:904225839"
variation 1469
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:780086534"
variation 1472
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231617308"
variation 1473
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788722421"
variation 1475
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750402593"
variation 1476
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788722188"
variation 1479
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:374698888"
variation 1481
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754390011"
variation 1484
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374903990"
variation 1485
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764595382"
variation 1488
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:760927946"
variation 1491
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1392045539"
variation 1492
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:751247222"
variation 1493
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:765908460"
variation 1497
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231728063"
variation 1499
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:762532256"
variation 1501
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:772655914"
variation 1503
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788721160"
variation 1508
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1352595882"
variation 1509
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:998280618"
variation 1510
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788720883"
variation 1511
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788720799"
variation 1514
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:769283721"
variation 1515
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338917076"
variation 1521
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:761808584"
variation 1523
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788720575"
variation 1524
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416971164"
variation 1525
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239558569"
variation 1528
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:371467779"
variation 1530
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:375808408"
variation 1531
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:372527866"
variation 1536
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199226836"
variation 1537
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1226769535"
variation 1539
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:370016963"
variation 1540
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:548655885"
variation 1542
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1732342289"
variation 1546
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:746088884"
variation 1551
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:868413594"
variation 1552
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:199668711"
variation 1553
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1005768906"
variation 1558
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779199736"
variation 1562
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:757383562"
variation 1563
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:79217348"
variation 1564
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241041655"
variation 1566
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382085642"
variation 1567
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788719040"
variation 1572
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:754447237"
variation 1573
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584034971"
variation 1579
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:919334631"
variation 1580
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397735614"
variation 1581
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788718621"
variation 1583..1589
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="att"
/replace="attgatt"
/db_xref="dbSNP:748022405"
variation 1583
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:140161690"
variation 1586
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788718480"
variation 1588
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788718405"
variation 1591
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:778376185"
variation 1594
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788718182"
variation 1597
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788718117"
variation 1601
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150882494"
variation 1603
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788717965"
variation 1607
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:34803612"
variation 1613
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:766074136"
exon 1614..1754
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1615..1616
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1200321533"
variation 1621
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788688123"
variation 1623
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114446805"
variation 1626
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427520406"
variation 1628
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357109733"
variation 1629
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584033824"
variation 1632
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:753283561"
variation 1634
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1158808236"
variation 1647
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364770988"
variation 1651
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:763645667"
variation 1652
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342253758"
variation 1654
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775464255"
variation 1655
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:148650117"
variation 1657
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:889456708"
variation 1660
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759358228"
variation 1663
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325105704"
variation 1664
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:74353230"
variation 1665
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1405482753"
variation 1666
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788686695"
variation 1670
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1395112257"
variation 1677
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:774745215"
variation 1678
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:771211647"
variation 1682
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:749396735"
variation 1683
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048557931"
variation 1687
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773226477"
variation 1688
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403798551"
variation 1691
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:769915140"
variation 1694
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1293669890"
variation 1696
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201254956"
variation 1698
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:748645425"
variation 1705
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:781686114"
variation 1707
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196756296"
variation 1709..1710
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1221750080"
variation 1709
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369262971"
variation 1712
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1305970890"
variation 1715
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:143946112"
variation 1716
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565399225"
variation 1717
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:940348303"
variation 1720..1724
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1248579679"
variation 1723
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223305496"
variation 1724
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:747303231"
variation 1727
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:778546389"
variation 1739
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:756960625"
variation 1740..1741
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="aa"
/db_xref="dbSNP:1788684608"
variation 1741
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1479757608"
variation 1742
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:767671391"
variation 1744
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436776564"
variation 1748
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:753484384"
variation 1749
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:201000981"
variation 1753
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584033628"
exon 1755..1879
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1755
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210625615"
variation 1756
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788343764"
variation 1760
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:368480640"
variation 1761
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:776825955"
variation 1763
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:12197456"
variation 1767
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:932045080"
variation 1771
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788343272"
variation 1772
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114428148"
variation 1779
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313745631"
variation 1780
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023276017"
variation 1785
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:761209858"
variation 1788
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:775954068"
variation 1790
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:772447981"
variation 1791
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:370173061"
variation 1792
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:960685672"
variation 1799
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788342532"
variation 1801
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:137871841"
variation 1802
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375152621"
variation 1803
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421783946"
variation 1805
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:556803789"
variation 1808
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1164188132"
variation 1810
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:780919086"
variation 1812
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788341940"
variation 1815
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415958105"
variation 1816
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182354105"
variation 1818
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754508624"
variation 1822
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:982698635"
variation 1829..1830
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="tta"
/db_xref="dbSNP:1260806043"
variation 1829
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455047701"
variation 1833
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379862423"
variation 1838..1841
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:35764647"
variation 1842..1843
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="ggtctcaatatgttgc"
/db_xref="dbSNP:1788341291"
variation 1842
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195497690"
variation 1844
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:746996203"
variation 1845..1846
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ag"
/replace="aggctgttctcaaacttctgggctcaag"
/db_xref="dbSNP:1788341076"
variation 1845
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264483358"
variation 1849..1850
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="at"
/db_xref="dbSNP:1292697064"
variation 1849
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218831431"
variation 1850
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780095002"
variation 1851
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788340803"
variation 1852
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1234459828"
variation 1854
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340405055"
variation 1856
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156234501"
variation 1857
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145208792"
variation 1861
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:750170950"
variation 1862
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:764925150"
variation 1868
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:757563152"
variation 1870
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1434463386"
variation 1872
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351710827"
variation 1874
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788340022"
exon 1880..1941
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1883
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1742566016"
variation 1884
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:893979296"
variation 1887
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:745866185"
variation 1889
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788256832"
variation 1890
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468992872"
variation 1894
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1374739339"
variation 1896
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054110814"
variation 1899
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788256514"
variation 1904..1908
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:753558498"
variation 1905
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231451987"
variation 1906
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469893789"
variation 1907..1911
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:1788255938"
variation 1907
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178143435"
variation 1909
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562674392"
variation 1910
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:778665307"
variation 1911
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:770790096"
variation 1912..1918
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:866380047"
variation 1913
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:749014790"
variation 1916
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474526868"
variation 1919
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788255549"
variation 1921
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:138622213"
variation 1930
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788255394"
variation 1931
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584016678"
variation 1938
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:756386744"
variation 1939
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365725293"
variation 1941
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:752913693"
exon 1942..4414
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/inference="alignment:Splign:2.1.0"
variation 1943
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:150140819"
variation 1944
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1158701299"
variation 1945
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:748421816"
variation 1947
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:781224670"
variation 1948
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:755121090"
variation 1952
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:751530044"
variation 1953
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388046612"
variation 1955..1963
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tgatga"
/replace="tgatgatga"
/db_xref="dbSNP:763277529"
variation 1958
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:780165684"
variation 1960
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788226773"
variation 1961
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:2114421159"
variation 1965
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759036505"
variation 1966
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487440320"
variation 1970
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:750926786"
variation 1971
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205862926"
variation 1974
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:765743612"
variation 1976
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1263665090"
variation 1977
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788226177"
variation 1981..1985
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tat"
/replace="tatat"
/db_xref="dbSNP:1788225953"
variation 1982
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:762218871"
variation 1984
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788226022"
variation 1995
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788225885"
variation 1999
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788225819"
variation 2005
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1369227295"
variation 2005
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1322869823"
variation 2006
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1562673631"
variation 2007
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788225484"
variation 2010
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1335320460"
variation 2021
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:752424330"
variation 2026
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:767011461"
variation 2027
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:374372548"
variation 2028
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:375253535"
variation 2030..2033
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gtag"
/replace="gtagtag"
/db_xref="dbSNP:1788225041"
variation 2033
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1275915835"
variation 2041..2045
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aa"
/replace="aacaa"
/db_xref="dbSNP:1239437685"
variation 2046
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1562673589"
variation 2047
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:773792900"
variation 2048
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788224685"
variation 2049
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347793150"
variation 2050
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="c"
/db_xref="dbSNP:774573467"
variation 2053
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:770424811"
variation 2057
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:762920471"
variation 2058
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788224397"
variation 2059
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:537118596"
variation 2062
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:769601753"
variation 2066
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1419143908"
variation 2072
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:747861313"
variation 2073..2074
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="ca"
/db_xref="dbSNP:1788223849"
variation 2074..2078
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="at"
/replace="ataat"
/db_xref="dbSNP:1194143002"
variation 2074..2076
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="ata"
/db_xref="dbSNP:1265668963"
variation 2074
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477045126"
variation 2075
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788223687"
variation 2078..2079
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tt"
/db_xref="dbSNP:753113679"
variation 2084
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:776920237"
variation 2092
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038505965"
variation 2102
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788223348"
variation 2103
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788223286"
variation 2110
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:759753616"
variation 2113
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1248457696"
variation 2114
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788223100"
variation 2115
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:764901787"
variation 2117
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:908801317"
variation 2121
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210338792"
variation 2122
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:533476180"
variation 2123
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208962578"
variation 2127
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:992159685"
variation 2132
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:951502616"
variation 2133
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:939373225"
variation 2135
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584015093"
variation 2138
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788222584"
variation 2139
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:559439723"
variation 2145
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197932192"
variation 2146
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788222404"
variation 2153
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584015078"
variation 2154
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="t"
/db_xref="dbSNP:1378093346"
variation 2157..2162
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ct"
/replace="ctctct"
/db_xref="dbSNP:536701101"
variation 2158
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:547808379"
variation 2161
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788222167"
variation 2166
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788222034"
variation 2175
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411310826"
variation 2178
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457894859"
variation 2180
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788221848"
variation 2182
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788221768"
variation 2187
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322728198"
variation 2188
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788221652"
variation 2190
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584015048"
variation 2191
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1388860611"
variation 2195
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788221484"
variation 2197
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016342211"
variation 2198
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298496215"
variation 2202
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324586932"
variation 2205
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:529340512"
variation 2206..2213
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="atta"
/replace="attaatta"
/db_xref="dbSNP:1228486248"
variation 2206
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:968127057"
variation 2208
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1366516691"
variation 2220
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1323021398"
variation 2221
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:561146429"
variation 2223..2231
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttatta"
/replace="ttattatta"
/db_xref="dbSNP:111625877"
variation 2223..2224
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1554330820"
variation 2224..2226
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tat"
/replace="tatat"
/db_xref="dbSNP:1554330819"
variation 2227
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788220799"
variation 2228
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1007259367"
variation 2229
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584014999"
variation 2233..2240
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:1030163834"
variation 2237
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788220555"
variation 2239
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303644826"
variation 2241
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1453168349"
variation 2243
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788220235"
variation 2246
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250990807"
variation 2247..2253
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gag"
/replace="gagtgag"
/db_xref="dbSNP:548363812"
variation 2247
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472923373"
variation 2249
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:542965893"
variation 2250
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788219977"
variation 2252..2257
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="agagta"
/db_xref="dbSNP:1428229363"
variation 2253
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366839635"
variation 2255
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:118086339"
variation 2256
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393324876"
variation 2257
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788219591"
variation 2259
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788219543"
variation 2264
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788219489"
variation 2265..2271
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tta"
/replace="ttaatta"
/db_xref="dbSNP:567579596"
variation 2276
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788219354"
variation 2279
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351669809"
variation 2289
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788219251"
variation 2293
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788219189"
variation 2296
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390698941"
variation 2297
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788219070"
variation 2301
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114420787"
variation 2304
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788219006"
variation 2305
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:989995145"
variation 2307
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1409860567"
variation 2309
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:182548046"
variation 2311
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308478967"
variation 2312
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788218706"
variation 2315
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338240153"
variation 2320
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788218606"
variation 2323
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052247605"
variation 2324..2334
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttttttttt"
/replace="tttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/db_xref="dbSNP:1265730491"
variation 2334
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:955967248"
variation 2339..2342
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1788218225"
variation 2339
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202776252"
variation 2340
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032027287"
variation 2343
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273758460"
variation 2347
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483326832"
variation 2349..2358
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tcttc"
/replace="tcttctcttc"
/db_xref="dbSNP:775243494"
variation 2353
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:544733751"
variation 2356
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:768295028"
variation 2358..2360
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1788217811"
variation 2359
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788217878"
variation 2362
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788217747"
variation 2374
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423388671"
variation 2388
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1045565825"
variation 2394
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788217542"
variation 2396
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370432936"
variation 2399
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584014825"
variation 2401
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788217393"
variation 2403
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114420682"
variation 2404
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:577666040"
variation 2405
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:117685592"
variation 2408..2424
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="ctctattacctcctcac"
/db_xref="dbSNP:1788216817"
variation 2412
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027955220"
variation 2413
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:996516501"
variation 2415
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="a"
/db_xref="dbSNP:1371602522"
variation 2417
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788216979"
variation 2419
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432145250"
variation 2423
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260707515"
variation 2425
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:917941804"
variation 2427
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1394948322"
variation 2432
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:540605992"
variation 2433
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:898270547"
variation 2435
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312910805"
variation 2436
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788216448"
variation 2439
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384568272"
variation 2445
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225779629"
variation 2448
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484005234"
variation 2449
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788216193"
variation 2450
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788216142"
variation 2454
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342684364"
variation 2457
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056705042"
variation 2458
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1038472853"
variation 2459
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:566010492"
variation 2460
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:918742428"
variation 2462
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788215791"
variation 2465
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788215741"
variation 2468..2472
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aa"
/replace="aacaa"
/db_xref="dbSNP:1258483803"
variation 2469
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:148391354"
variation 2476
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447854240"
variation 2477
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1188221312"
variation 2479
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1232896122"
variation 2482
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788215133"
variation 2487
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788215084"
variation 2488
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788215027"
variation 2492
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:555608903"
variation 2505
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:537362192"
variation 2508..2511
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1788214844"
variation 2511
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:887350469"
variation 2513
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451791335"
variation 2514
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:908926118"
variation 2516..2517
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1788214587"
variation 2524
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057158029"
variation 2527
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="a"
/db_xref="dbSNP:566787231"
variation 2527
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377568353"
variation 2529
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302949483"
variation 2540
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:13213236"
variation 2541
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:558333838"
variation 2548
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432434365"
variation 2559
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319556664"
variation 2563
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="c"
/db_xref="dbSNP:1788213874"
variation 2564..2566
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2114420488"
variation 2564
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:146179029"
variation 2569
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788213741"
variation 2571
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:953048805"
variation 2577
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:566154372"
variation 2581
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788213573"
variation 2582
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:547939834"
variation 2584
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029967081"
variation 2585
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233932487"
variation 2586
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:926571000"
variation 2587
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1045109366"
variation 2590
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114420454"
variation 2595
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:143201026"
variation 2597
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788213134"
variation 2602
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788213091"
variation 2604
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788213025"
variation 2606
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1208339708"
variation 2607
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248883208"
variation 2608
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:371455695"
variation 2610
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788212808"
variation 2611
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487019448"
variation 2614
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114420427"
variation 2615
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:915355777"
variation 2620
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:989979446"
variation 2625
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788212549"
variation 2627
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030788703"
variation 2629
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788212431"
variation 2630..2637
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttttttt"
/replace="tttttttt"
/replace="ttttttttt"
/db_xref="dbSNP:546948534"
variation 2633
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:956105266"
variation 2640
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114420386"
variation 2644
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:568481387"
variation 2645
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788212079"
variation 2648
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788211997"
variation 2651
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432590522"
variation 2654
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1430484665"
variation 2661
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="a"
/db_xref="dbSNP:1372413315"
variation 2664
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788211612"
variation 2665..2671
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="ccgtatc"
/db_xref="dbSNP:1285185653"
variation 2666
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:549258695"
variation 2667
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:771504990"
variation 2668
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387265193"
variation 2669
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788211361"
variation 2673
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788211237"
variation 2674
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:532853509"
variation 2675
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:189523254"
variation 2676
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1372319218"
variation 2677
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:6913331"
variation 2685
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788210886"
variation 2689
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:139853137"
variation 2691
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788210723"
variation 2693
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016662831"
variation 2697
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:780889806"
variation 2698
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788210564"
variation 2700
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788210503"
variation 2704
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114420282"
variation 2705
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788210436"
variation 2707
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219691111"
variation 2709
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:896478367"
variation 2713
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788210084"
variation 2714
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489052126"
variation 2716
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1202144207"
variation 2721
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254941435"
variation 2725
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788209846"
variation 2733
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788209795"
variation 2737
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004383302"
variation 2738
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788209728"
variation 2739
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788209655"
variation 2740
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180869542"
variation 2742..2751
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aataaa"
/replace="aataaataaa"
/db_xref="dbSNP:1209608170"
variation 2743
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562673162"
variation 2747
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788209479"
variation 2748
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114420234"
variation 2749..2752
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1788209346"
variation 2753
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402063667"
variation 2756
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788209247"
variation 2757..2759
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:930210744"
variation 2757
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:565089869"
variation 2758
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162329487"
variation 2759
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056504831"
variation 2771
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788208927"
variation 2774
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:185147825"
variation 2781
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788208819"
variation 2782
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897447120"
variation 2784
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788208685"
variation 2785
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788208630"
variation 2787
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:887309084"
variation 2788
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039032421"
variation 2790..2791
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="aa"
/db_xref="dbSNP:1788208395"
variation 2790
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1203678664"
variation 2791
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788208345"
variation 2792
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056637497"
variation 2794
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1375697844"
variation 2796
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226822382"
variation 2797
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:941497960"
variation 2802
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788208091"
variation 2803..2804
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="cc"
/replace="tg"
/db_xref="dbSNP:386705765"
variation 2803
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:562076398"
variation 2804
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:541824731"
variation 2809
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788207850"
variation 2811
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:931752827"
variation 2812
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:184005307"
variation 2814..2820
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tct"
/replace="tctgtct"
/db_xref="dbSNP:2114420134"
variation 2815
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1292911135"
variation 2816
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="t"
/db_xref="dbSNP:1410606162"
variation 2816
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232940297"
variation 2819
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788207526"
variation 2821
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788207438"
variation 2824
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352430751"
variation 2826
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179680395"
variation 2827
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788207274"
variation 2829
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788207215"
variation 2830
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:946721554"
variation 2834
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306217886"
variation 2835
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1408177012"
variation 2838
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:975759181"
variation 2839
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:915323259"
variation 2840
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:540746542"
variation 2841
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428998950"
variation 2846..2849
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1788206763"
variation 2848
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:192057503"
variation 2849
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:979777057"
variation 2851
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573265661"
variation 2852
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788206528"
variation 2853
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788206473"
variation 2858
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283771105"
variation 2860
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380209205"
variation 2862..2864
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttt"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1248496618"
variation 2866
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:554950379"
variation 2867
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206492485"
variation 2868
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159812102"
variation 2869
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1438983364"
variation 2875
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012316831"
variation 2877
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788205924"
variation 2880
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788205867"
variation 2885
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:924402227"
variation 2887
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788205759"
variation 2894
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236492086"
variation 2897
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584014297"
variation 2898
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788205600"
variation 2900
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788205538"
variation 2901
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788205485"
variation 2902
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:986672382"
variation 2905
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:186964684"
variation 2906
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:543800350"
variation 2910
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:576668812"
variation 2913
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:962394127"
variation 2919
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788205108"
variation 2925
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:145975637"
variation 2928
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788204994"
variation 2929
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788204936"
variation 2931
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:982899666"
variation 2933
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788204844"
variation 2937
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584014250"
variation 2940
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:181883768"
variation 2943
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788204655"
variation 2946
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333558182"
variation 2947
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1268664480"
variation 2948
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1035568956"
variation 2949..2959
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttttttt"
/replace="tttttttttt"
/replace="ttttttttttt"
/replace="tttttttttttt"
/replace="ttttttttttttt"
/replace="tttttttttttttt"
/db_xref="dbSNP:rs60420681"
variation 2950
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788204451"
variation 2953
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788204401"
variation 2959
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788204169"
variation 2960
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219195047"
variation 2963
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1562672960"
variation 2964
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003743511"
variation 2969
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212086323"
variation 2976
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:190280860"
variation 2977
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1023929956"
variation 2978
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788203784"
variation 2980
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323693817"
variation 2981
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788203676"
variation 2982
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788203615"
variation 2985
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788203553"
variation 2986
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788203506"
variation 2987
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788203457"
variation 2990..2996
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttct"
/replace="ttcttct"
/db_xref="dbSNP:1245832877"
variation 2996
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050371352"
variation 2997..2999
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:923057716"
variation 2998
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:931728668"
variation 3005
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243674110"
variation 3006
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1010902704"
variation 3007
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="g"
/db_xref="dbSNP:1171987632"
variation 3009..3012
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="tttt"
/db_xref="dbSNP:975808161"
variation 3010
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419860"
variation 3015
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788202915"
variation 3017
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788202861"
variation 3020..3024
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1584014138"
variation 3025
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331446581"
variation 3031
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788202678"
variation 3032
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470999086"
variation 3037
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:531706123"
variation 3038
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:78506382"
variation 3040
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788202378"
variation 3045
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441545883"
variation 3049
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788202254"
variation 3057
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:2114419808"
variation 3058
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788202194"
variation 3062
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419806"
variation 3067
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329756706"
variation 3072
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335165906"
variation 3076
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275969497"
variation 3080
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224848756"
variation 3090
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:535964199"
variation 3093
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788201766"
variation 3099
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265810550"
variation 3102
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328013442"
variation 3106
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205407411"
variation 3115
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286071893"
variation 3116
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788201514"
variation 3118
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449723236"
variation 3119
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562672871"
variation 3122
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197997003"
variation 3125
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:746571825"
variation 3127
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788201247"
variation 3136
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788201175"
variation 3138
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269535044"
variation 3141
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324128759"
variation 3142
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1481430966"
variation 3143..3147
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="aagta"
/db_xref="dbSNP:779442659"
variation 3145
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180146301"
variation 3153
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388382821"
variation 3163..3166
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1562672839"
variation 3166..3168
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1392045158"
variation 3167
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1454479366"
variation 3170
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389016280"
variation 3171
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405156776"
variation 3178
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:935391976"
variation 3182
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304233036"
regulatory 3186..3191
/regulatory_class="polyA_signal_sequence"
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="hexamer: AATAAA"
variation 3187
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788198471"
variation 3194
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788198414"
variation 3198
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347974653"
variation 3199
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408583270"
variation 3205
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788198244"
variation 3209
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285886040"
variation 3211
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419728"
variation 3212
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788198151"
variation 3213
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788198096"
polyA_site 3214
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="major polyA site"
variation 3215
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788198048"
variation 3219
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:568419607"
variation 3220
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:979360994"
variation 3221
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:890560118"
variation 3226..3230
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="catga"
/replace="catgacatga"
/db_xref="dbSNP:542025867"
variation 3226
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457492918"
variation 3228
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353921571"
variation 3230
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:550197790"
variation 3233
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="c"
/db_xref="dbSNP:1490811130"
variation 3236
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469187061"
variation 3237
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788197392"
variation 3239
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114419689"
variation 3240
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788197318"
variation 3244
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:933851550"
variation 3246
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035062294"
variation 3248
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788197140"
variation 3251
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788197083"
variation 3256
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562672785"
variation 3257
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419669"
variation 3258
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:531652109"
variation 3259
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788196516"
variation 3260
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246726352"
variation 3263
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788196377"
variation 3282
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:980257208"
variation 3283..3287
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1472653663"
variation 3287
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788196175"
variation 3288
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164577180"
variation 3292..3293
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1788196044"
variation 3294..3300
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gggggg"
/replace="ggggggg"
/replace="gggggggg"
/replace="ggggggggg"
/db_xref="dbSNP:1005783053"
variation 3295
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569919863"
variation 3296
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308035384"
variation 3297
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551412735"
variation 3298
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788195718"
variation 3299
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788195662"
variation 3300
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1391475532"
variation 3301
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788195402"
variation 3302
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:890072671"
variation 3306
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049915144"
variation 3311
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273829255"
variation 3321
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788195132"
variation 3334
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788195072"
variation 3336
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480974403"
variation 3338
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118248"
variation 3342
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:368488473"
variation 3345
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562672728"
variation 3350
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584013840"
variation 3351
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:76725375"
variation 3354..3355
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="cc"
/replace="cccc"
/db_xref="dbSNP:778390994"
variation 3355
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788194601"
variation 3356
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788194542"
variation 3357
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:909514371"
variation 3360
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788194432"
variation 3363
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184501899"
variation 3364
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387468310"
variation 3368
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448051906"
variation 3369
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1282415718"
variation 3370
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788194084"
variation 3375
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223362985"
variation 3376
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374164935"
variation 3377
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:11544373"
variation 3383..3388
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="gtg"
/replace="gtggtg"
/db_xref="dbSNP:1299355056"
variation 3383
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788193794"
variation 3390
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276636550"
variation 3392
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:528958448"
variation 3393
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1337056604"
variation 3395
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235383004"
variation 3396
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:935112140"
variation 3398..3400
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="att"
/db_xref="dbSNP:1584013767"
variation 3401
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:923614833"
variation 3402
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1307977906"
variation 3411
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788192905"
variation 3412
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788192845"
variation 3413..3416
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1788192803"
variation 3419
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788192730"
variation 3423
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:561492298"
variation 3426
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:2114419469"
variation 3427
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:755184460"
regulatory 3429..3434
/regulatory_class="polyA_signal_sequence"
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="hexamer: ATTAAA"
variation 3436
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:946648792"
variation 3437
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788192499"
variation 3443
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788192450"
variation 3446..3448
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1390481206"
variation 3446
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323007797"
polyA_site 3451
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="major polyA site"
variation 3451
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788192191"
variation 3455..3459
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1399707295"
variation 3455
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315804180"
variation 3456
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788192093"
variation 3457
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:951192382"
variation 3458
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1463785646"
variation 3459..3460
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="tt"
/db_xref="dbSNP:1425300053"
variation 3464
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562672646"
variation 3466
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788191813"
variation 3471
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262917449"
variation 3475
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:149500865"
variation 3477
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:916451883"
variation 3483
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419404"
variation 3489..3491
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1468835387"
variation 3489
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:982271380"
variation 3491
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788191520"
variation 3493
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:990736069"
variation 3494
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173788870"
variation 3496
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407887444"
variation 3497..3501
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1584013659"
variation 3500
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788191316"
variation 3504..3512
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttttttt"
/replace="tttttttt"
/replace="ttttttttt"
/replace="tttttttttt"
/db_xref="dbSNP:35010083"
variation 3507
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584013654"
variation 3509
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:41285294"
variation 3511
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1023815506"
variation 3512
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:564773625"
variation 3513
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:961783289"
variation 3514
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788190707"
variation 3516..3523
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aatattga"
/db_xref="dbSNP:1215396154"
variation 3520
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016933224"
variation 3523
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:138039665"
variation 3525..3527
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1487090594"
variation 3525
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261665062"
variation 3527
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788190363"
variation 3529
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788190301"
variation 3530
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240663980"
variation 3533..3538
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tttt"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1479794751"
variation 3533
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215354480"
variation 3539
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199472308"
variation 3545
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430859673"
variation 3546
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114419303"
variation 3553
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031394035"
variation 3554
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1443171703"
variation 3555..3571
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tctattttct"
/replace="tctattttctattttct"
/db_xref="dbSNP:1345726618"
variation 3556
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:369024980"
variation 3558
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:150785533"
variation 3565
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:554410133"
variation 3568
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208806735"
variation 3578
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1302594468"
variation 3584
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028970780"
variation 3589
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788189254"
variation 3590
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:558265359"
variation 3596
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788189161"
variation 3598
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788189107"
variation 3603
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285247861"
variation 3606
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419259"
variation 3613
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:998408151"
variation 3618
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:756334107"
variation 3619
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:113572799"
variation 3622
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788188664"
variation 3624
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:574979073"
variation 3634
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1219851253"
variation 3635
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:556732278"
variation 3643
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:181349835"
variation 3644
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359358077"
variation 3650
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788188312"
variation 3651..3656
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttc"
/replace="ttcttc"
/db_xref="dbSNP:1788188137"
variation 3653
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788188260"
variation 3654
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:902297749"
variation 3659
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788188082"
variation 3661
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1043492894"
variation 3667
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788187974"
variation 3670
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788187927"
variation 3671
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432320355"
variation 3673
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788187808"
variation 3674
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788187754"
variation 3675
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788187709"
variation 3677
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1039529577"
variation 3681
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374251052"
variation 3693
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788187534"
variation 3695
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788187479"
variation 3698
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169795138"
variation 3699
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788187373"
variation 3701
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451821633"
variation 3704
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417847804"
variation 3710
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186275554"
variation 3711
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:141344897"
variation 3713
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:909829196"
variation 3715
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:982836198"
variation 3717
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368707094"
variation 3718
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1185998350"
variation 3725
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:551615836"
variation 3729
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788186859"
variation 3731
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788186807"
variation 3735
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:758444205"
variation 3740
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114419120"
variation 3742
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788186707"
variation 3747
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1441576813"
variation 3748..3754
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aat"
/replace="aattaat"
/db_xref="dbSNP:939275991"
variation 3748..3750
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="aat"
/db_xref="dbSNP:1788186539"
variation 3749
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788186588"
variation 3752
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:916265182"
variation 3754
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1055018111"
variation 3755
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584013345"
variation 3758..3763
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="ataaaa"
/db_xref="dbSNP:1273122920"
variation 3760
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:929694782"
variation 3762
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584013335"
variation 3763
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:188150005"
variation 3774
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:961475226"
variation 3775
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203248414"
variation 3777
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309154869"
variation 3786..3789
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1788185666"
variation 3786
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788185716"
variation 3793
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270681513"
variation 3794
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:981822752"
variation 3796
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213759237"
variation 3797
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788185429"
variation 3800
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584013311"
variation 3803
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281288502"
variation 3805
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788185265"
variation 3806..3814
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/replace="aaaaaaaaaa"
/replace="aaaaaaaaaaaaaa"
/db_xref="dbSNP:113680268"
variation 3807
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:909922723"
variation 3813
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788185139"
variation 3814
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294749626"
variation 3815
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417320023"
variation 3816
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1171201587"
variation 3818..3822
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ag"
/replace="agcag"
/db_xref="dbSNP:1788184712"
variation 3820
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:750381033"
variation 3821..3826
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="agtgag"
/replace="agtgagtgag"
/db_xref="dbSNP:1383912025"
variation 3821
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:916728838"
variation 3827
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336332126"
variation 3830
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354288520"
variation 3832
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788184486"
variation 3834
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788184416"
variation 3835
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:765323194"
variation 3836
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788182379"
variation 3840
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:761853115"
variation 3842
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:183919403"
variation 3843
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:554271856"
variation 3846
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:367631564"
variation 3847
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:193230540"
variation 3848
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788182003"
variation 3850
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308816764"
variation 3856
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788181910"
variation 3857
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788181873"
variation 3860
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353259170"
variation 3861
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242156291"
variation 3864
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1170273008"
variation 3876
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:753618856"
variation 3877
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561430985"
variation 3880
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:996179183"
variation 3881
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114073692"
variation 3882
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:759662636"
variation 3884
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:998946589"
variation 3886
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788181283"
variation 3889
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421662841"
variation 3890
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788181178"
variation 3898..3901
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1788181067"
variation 3899
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1474980238"
variation 3905
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468311279"
variation 3906
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:904694177"
variation 3908
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788180927"
variation 3911
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788180884"
variation 3922
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1407154099"
variation 3926..3929
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="at"
/replace="atat"
/db_xref="dbSNP:1788180669"
variation 3926
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788180775"
variation 3928
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788180715"
variation 3934
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788180596"
variation 3935
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1022438908"
variation 3939
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1252680957"
variation 3945..3968
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="agtatcttaattttaaaaaagtga"
/db_xref="dbSNP:1788180013"
variation 3945
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326267998"
variation 3947..3949
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tat"
/db_xref="dbSNP:777445618"
variation 3948
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432100651"
variation 3950
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1184411970"
variation 3959..3964
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1010667061"
variation 3959
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1363379174"
variation 3964
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788180062"
variation 3966
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1039498401"
variation 3967
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481608520"
variation 3968
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:763827652"
variation 3973
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205243542"
variation 3974
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788179878"
variation 3992
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:138971307"
variation 3994
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1054817645"
variation 4000
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193739144"
variation 4004
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788179646"
variation 4005
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:888358898"
variation 4006
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="g"
/db_xref="dbSNP:1788179529"
variation 4006
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:939246602"
variation 4013
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:563936154"
variation 4016
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788179330"
variation 4017
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788179279"
variation 4021
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036957385"
variation 4022
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:929887874"
variation 4024..4025
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1788179081"
variation 4024
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:927611194"
variation 4028
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320794266"
variation 4029
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788178982"
variation 4032
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:535962790"
variation 4034
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1404922342"
variation 4035
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788178816"
variation 4036
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788178756"
variation 4037
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:546430761"
variation 4038
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288498631"
variation 4045
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788178575"
variation 4046
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392624518"
variation 4048
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788178486"
variation 4049..4055
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1224898595"
variation 4051
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788178283"
variation 4056
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="t"
/db_xref="dbSNP:1277424378"
variation 4058
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349622869"
variation 4060
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584013018"
variation 4062
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:947758817"
variation 4066..4071
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1205537990"
variation 4075
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2114418692"
variation 4076
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788177885"
variation 4077
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:916365176"
variation 4083
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:572776603"
variation 4089
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1269686695"
variation 4090
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490861269"
variation 4093..4095
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="ggt"
/db_xref="dbSNP:1788177401"
variation 4093
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:976757067"
variation 4094
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363462789"
variation 4095
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470693996"
variation 4097..4098
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:753115615"
variation 4097
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788177276"
variation 4100
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:565899088"
variation 4101
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397182807"
variation 4102
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788177045"
variation 4106
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1383829196"
variation 4109
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788176992"
variation 4110
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:958270341"
variation 4111
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584012955"
variation 4112
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788176834"
variation 4113
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788176784"
variation 4117
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1424583111"
variation 4119
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:147032368"
variation 4122
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788176602"
variation 4125
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788176543"
variation 4129
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788176482"
variation 4130
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461168121"
variation 4133
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365599167"
variation 4134
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584012929"
variation 4135
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:141576097"
variation 4136
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775054997"
variation 4137
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417407613"
variation 4138
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021821015"
variation 4142
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:955133193"
variation 4143
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1030260218"
variation 4149
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788175779"
variation 4150..4171
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ctcaagca"
/replace="ctcaagcactggggctcaagca"
/db_xref="dbSNP:1788175182"
variation 4152
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1488741240"
variation 4153
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245069288"
variation 4155
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:996161352"
variation 4156
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:2114418580"
variation 4160..4163
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1788175512"
variation 4163
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788175454"
variation 4164
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788175399"
variation 4169
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211561456"
variation 4170
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467807706"
variation 4176
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788175125"
variation 4177
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194181783"
variation 4178
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268377646"
variation 4179
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788174937"
variation 4188
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:964746887"
variation 4190
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240673849"
variation 4191
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314642088"
variation 4195
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1033336603"
variation 4198
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788174316"
variation 4199
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788174251"
variation 4201
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114418524"
variation 4203
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305624429"
variation 4206
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788174128"
variation 4210
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788174073"
variation 4211
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016341785"
variation 4216
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:796812841"
variation 4218
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1005788180"
variation 4223
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324368378"
variation 4226
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1165632522"
variation 4229
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:2114418502"
variation 4230
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395220225"
variation 4234
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788173702"
variation 4241..4248
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:551491295"
variation 4242
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391605851"
variation 4248..4249
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="g"
/db_xref="dbSNP:1684384517"
variation 4248
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1788173487"
variation 4250
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380225503"
variation 4252
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562672117"
variation 4258
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:888250592"
variation 4261
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1047338112"
variation 4264
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788173243"
variation 4265
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788173184"
variation 4268
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1315596313"
variation 4275
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:771580885"
variation 4278
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:139113766"
variation 4279
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1225212272"
variation 4280
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/db_xref="dbSNP:1788172878"
variation 4283
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1788172822"
variation 4292..4296
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ct"
/replace="ctact"
/db_xref="dbSNP:1250815855"
variation 4304
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:994074774"
variation 4308
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1343322949"
variation 4310..4317
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tttttttt"
/replace="ttttttttt"
/db_xref="dbSNP:532871101"
variation 4310
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584012747"
variation 4311
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788172518"
variation 4315
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788172475"
variation 4320
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1261523768"
variation 4323
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788172295"
variation 4324
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584012731"
variation 4326
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:906464103"
variation 4327
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046085762"
variation 4335
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:556664808"
variation 4336
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1184562702"
variation 4340
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:6901510"
variation 4341
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:916332824"
variation 4349..4355
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttt"
/replace="tttattt"
/db_xref="dbSNP:1048264547"
variation 4351
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:190569016"
variation 4353..4355
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1462059812"
variation 4356
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace=""
/replace="g"
/db_xref="dbSNP:142202741"
variation 4356
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584012669"
variation 4362
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:558681048"
variation 4364
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:932721807"
variation 4372
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788171391"
variation 4374
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:921315866"
variation 4375
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:936426349"
variation 4379..4387
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaaa"
/replace="aaaataaaa"
/db_xref="dbSNP:1454692381"
regulatory 4381..4386
/regulatory_class="polyA_signal_sequence"
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="hexamer: AATAAA"
variation 4381
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1381146716"
variation 4386..4394
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="aaata"
/replace="aaataaata"
/db_xref="dbSNP:1562672026"
variation 4387
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1380451993"
variation 4388
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327051434"
regulatory 4391..4396
/regulatory_class="polyA_signal_sequence"
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/note="hexamer: AATATA"
variation 4392..4397
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1220579248"
variation 4392
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788170955"
variation 4393
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:538914184"
variation 4396
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584012620"
variation 4398
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788170650"
polyA_site 4401
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
variation 4406
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:1788170604"
variation 4407
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="g"
/db_xref="dbSNP:1788170560"
variation 4408..4410
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1788170510"
variation 4410
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="t"
/db_xref="dbSNP:978685418"
variation 4411
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1788170373"
polyA_site 4414
/gene="ARHGAP18"
/gene_synonym="bA307O14.2; MacGAP; SENEX"
ORIGIN
ctctgtgtcaggatcgcagaaagtatgtcccttctctcaccatgagctggctctccagttcccagggagtggtactaacagcctaccaccccagcggcaaggaccagaccgtcgggaacagccatgcaaaggcaggggaggaagccacctcgagtcgcagatatggccagtacactatgaaccaggaaagcaccaccatcaaagttatggagaagcctccatttgatcgatcaatttcccaggattctttggatgaactatctatggaagactattggatagaactagaaaacatcaagaaatctagtgaaaacagccaagaagatcaagaggtggttgttgtcaaagagcctgatgagggagaattggaagaagagtggcttaaagaggccggtttatccaatctcttcggagagtctgctggagatccacaggaaagcattgtgtttttatcaacattgacgcggacccaggcagcagcagttcagaagcgagtagagacggtctcccagaccttgaggaaaaaaaacaaacagtaccagattcctgacgtcagagacatatttgctcaacagagagaatcaaaagaaacagctccaggtggcactgaatcgcagtcacttagaacaaatgaaaacaaataccaaggaagagatgacgaggcatctaaccttgttggtgaagagaagctgatcccacctgaggagacgcctgcccctgaaacagacatcaacctggaggtatcatttgccgagcaagcactcaatcagaaagagagctccaaggagaaaatccagaagagcaaaggcgatgatgccacattacctagtttcagattgccaaaagacaaaacgggtaccacaaggattggtgacctcgcaccccaggacatgaagaaagtttgccatttagccctaattgagctgactgccctctatgatgtattgggtattgagctgaaacaacaaaaagctgtgaaaatcaaaacaaaagattctggtcttttttgcgttccattgacagcgctattagaacaagatcagaggaaagtaccaggaatgcgaatacccttgatctttcaaaaactgatttctcgaattgaagagagaggtttggaaacagaaggcctcttacggatccctggagctgccattagaatcaagaatctttgccaagaactagaagcaaagttttatgaagggacttttaattgggaaagtgtcaaacagcatgatgccgccagcctgctgaagctcttcattcgggagttgccccagccactgctcagtgtggagtatctcaaagcctttcaggctgtccagaatcttccaaccaagaagcagcaactacaggctttgaaccttcttgtcatcctcctacctgatgcaaacagggacacactgaaggcccttcttgaatttctccaaagagtaatagataataaagaaaaaaataaaatgacagtcatgaatgtagcaatggtcatggccccgaatctctttatgtgtcatgcattgggattgaagtccagtgaacagcgagaatttgtaatggcagctgggacagcaaataccatgcacttattgattaagtaccaaaaacttctgtggacaattcccaagtttattgtaaaccaagtgaggaagcaaaacacggaaaatcataaaaaggataaaagagccatgaagaaattgctgaagaaaatggcttatgaccgagaaaaatatgaaaagcaagataagagtacaaatgatgctgacgttcctcagggagtgattcgagtgcaagctccccatctttcgaaagtttccatggcaatacagctaactgaagaactaaaagccagtgatgtacttgccaggtttctcagccaagaaagtggggttgcccagactctcaagaaaggagaagtttttttgtatgaaattggaggaaatattggggaacgctgccttgatgatgacacttacatgaaggatttatatcagcttaacccaaatgctgagtgggttataaagtcaaagccattgtagaagacttaacaagctgcagataaccatgtggacttctgtcataattcttgctgagtcaagagtgtaaataaaagaaatggcaggactcatattattcagttgtacccaagtatttaaaaatgactctcttaagccttaaaaagtcatagatttgtgctgctgccagaattatattaattattattaatgttattattagaaaaaaaatttctggagtgagagtaaagaggcttaattagtttgtgggcagttttcatatgctctgtgaaatgtgtccagatgtgacatagtttttttttttaatatgtggaaatgtcttctcttcccattcttttctcctaaaatcatatatactgtaatatatgctctctcacctctattacctcctcacatctaccctttcccagttaggtttgctttttgaccaaaaagataacaaataccaggtatggcaagttgtgaagacagcacattaaaacatacctaatttcacagtattcctgtcacgacagaatgttagtattcatctctttgaatcatttgctcaaataataacattccaccttttcctgctgtatcacaggaagtgatttgcattttttttcagttcatctgacttatgttcacagaaccgtatcagcgaccaagaaaataggactgtcagaagctgccagttattactgaaccattaaatacttatatactaagaataaataaaatatacccatgtgaaataataattggattatggataacaagagagtgaaagccaaagcactttctgtctactgtactcttctaaatggaattttaaaagtcatagctggctttacgtgttgtcattattagcattataaatatgcatgatagtataatccagtaatggttgaagaatgtattttacttaaagagggatttttttttttaagtcctgaataagtctactggaagaattattcttctgggtgaaaaagcttttgtttgtgttcttattttaaataatcggagtcaatttattaaaatgttcttgaaagtactattcccagggattttaatgcacaaaccatattgtgacaagagatgagcctctgtactgtaaataagaaatgaagtagagaaatgttaaatattttatgagtttagaatatagtaaataaaaggtgatgtaaatgaatgctgcacaaacggtgttcatgatacttttagtagtactttaggaaaaactacacattctcagaagctcttgatgtctctaatgaagggggggaatgctgttaatgagaacagtcataaatttttagcatataattacaagaacagcctgtggatatgatcacttaaatgattttgtggtgattcgtgccattgcttttttatttaaaagaaaattttgtaattaaatgcctttttctaaattatcttctcttggaatcattacttttaatcctatgtgtttatgagtatttttgctttttttttattaatattgagaaatggacttttttgttattaaaagtcacctctattttctattttctttgtaatttttaaagtaggaagatgtcagagatgtaaatatgttttcgtctttagtttttttccttttacaaatttttattcttcaggattttcaaaatacagtttagtctgtttctttgacaatatgtattaatttcccaattagcaaaatggtacttattagtgggttgaaaacaattaataatataaaagaaaaattaagtgcttaaaacattttaggagtatacaacttcaaaaaaaaagatagcagtgaggataatgatttaagtaaaaggttgtctgaagcatatgccaactaaatttcgcaacgtttgctacctacctgaaaaggagggtcaggagggagacacaacatatttttgatcatgaaaaagtatcttaattttaaaaaagtgaaaatgccattttattttgaatcccttttagaactcacgacccaagttcatcaatgttgaataatatcacgtttaaataacaaaaaaatatggactttaaaaaatctcaaattttttagagacagggtcttgctctgttttccagattggagtacagcagtgcattcgcggctaactgcagcctcaagcactggggctcaagcaaacctcctgcctcagcctcgtgagtagctaggaccacaggtgcatgccaccatgcctggctctaaagagaaaaaaaacttgataccatagagccttgaatataaatatcctgatgttaacctactgcttttgctgtgattttttttccttagtgagttttaaatctcaggctagatttttatttgtttttctgtgtgtgtatgagacaaaataaaaataaatatatttgccttgagtttaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]