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Previous release (v1)
2025-01-31 08:41:17, GGRNA.v2 : RefSeq release 227 (Nov, 2024)
LOCUS NM_018306 2025 bp mRNA linear PRI 06-JUN-2024
DEFINITION Homo sapiens transmembrane protein 40 (TMEM40), transcript variant
2, mRNA.
ACCESSION NM_018306
VERSION NM_018306.4
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 2025)
AUTHORS Lim,S.H., Snider,J., Birimberg-Schwartz,L., Ip,W., Serralha,J.C.,
Botelho,H.M., Lopes-Pacheco,M., Pinto,M.C., Moutaoufik,M.T.,
Zilocchi,M., Laselva,O., Esmaeili,M., Kotlyar,M., Lyakisheva,A.,
Tang,P., Lopez Vazquez,L., Akula,I., Aboualizadeh,F., Wong,V.,
Grozavu,I., Opacak-Bernardi,T., Yao,Z., Mendoza,M., Babu,M.,
Jurisica,I., Gonska,T., Bear,C.E., Amaral,M.D. and Stagljar,I.
TITLE CFTR interactome mapping using the mammalian membrane two-hybrid
high-throughput screening system
JOURNAL Mol Syst Biol 18 (2), e10629 (2022)
PUBMED 35156780
REFERENCE 2 (bases 1 to 2025)
AUTHORS Zhang,Q., Huang,D., Zhang,Z., Feng,Y., Fu,M., Wei,M., Zhou,J.,
Huang,Y., Liu,S. and Shi,R.
TITLE High expression of TMEM40 contributes to progressive features of
tongue squamous cell carcinoma
JOURNAL Oncol Rep 41 (1), 154-164 (2019)
PUBMED 30320346
REMARK GeneRIF: Study found that TMEM40 expression was increased in tongue
squamous cell carcinoma (TSCC) tissues and associated with
clinicopathological parameters. Further results indicated that
TMEM40 promoted TSCC development and progression via regulation of
p53, Bax and MMP9.
REFERENCE 3 (bases 1 to 2025)
AUTHORS Zhang,Z.F., Zhang,H.R., Zhang,Q.Y., Lai,S.Y., Feng,Y.Z., Zhou,Y.,
Zheng,S.R., Shi,R. and Zhou,J.Y.
TITLE High expression of TMEM40 is associated with the malignant behavior
and tumorigenesis in bladder cancer
JOURNAL J Transl Med 16 (1), 9 (2018)
PUBMED 29351801
REMARK GeneRIF: TMEM40 represents a potential oncogene, which exert a
crucial role in the proliferation and apoptosis via the p53
signaling pathway in bladder cancer.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 2025)
AUTHORS Pankow,S., Bamberger,C., Calzolari,D., Martinez-Bartolome,S.,
Lavallee-Adam,M., Balch,W.E. and Yates,J.R. 3rd.
TITLE F508 CFTR interactome remodelling promotes rescue of cystic
fibrosis
JOURNAL Nature 528 (7583), 510-516 (2015)
PUBMED 26618866
REFERENCE 5 (bases 1 to 2025)
AUTHORS Macaulay,I.C., Tijssen,M.R., Thijssen-Timmer,D.C., Gusnanto,A.,
Steward,M., Burns,P., Langford,C.F., Ellis,P.D., Dudbridge,F.,
Zwaginga,J.J., Watkins,N.A., van der Schoot,C.E. and Ouwehand,W.H.
TITLE Comparative gene expression profiling of in vitro differentiated
megakaryocytes and erythroblasts identifies novel activatory and
inhibitory platelet membrane proteins
JOURNAL Blood 109 (8), 3260-3269 (2007)
PUBMED 17192395
REFERENCE 6 (bases 1 to 2025)
AUTHORS Gevaert,K., Goethals,M., Martens,L., Van Damme,J., Staes,A.,
Thomas,G.R. and Vandekerckhove,J.
TITLE Exploring proteomes and analyzing protein processing by mass
spectrometric identification of sorted N-terminal peptides
JOURNAL Nat Biotechnol 21 (5), 566-569 (2003)
PUBMED 12665801
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK092470.1, AK001898.1, AI452552.1 and AC034198.7.
On Nov 23, 2018 this sequence version replaced NM_018306.3.
Transcript Variant: This variant (2) differs in the 5' UTR, lacks a
portion of the 5' coding region, and initiates translation at a
downstream in-frame start codon, compared to variant 1. The encoded
isoform (b) is shorter at the N-terminus, compared to isoform a.
##Evidence-Data-START##
Transcript exon combination :: AK092470.1, BX334345.2 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1968540,
SAMEA1968832 [ECO:0006172]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000314124.12/ ENSP00000322837.7
RefSeq Select criteria :: based on conservation, expression
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-859 AK092470.1 51-909
860-1360 AK001898.1 752-1252
1361-1660 AK092470.1 1411-1710
1661-2023 AI452552.1 5-367 c
2024-2025 AC034198.7 147822-147823
FEATURES Location/Qualifiers
source 1..2025
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3p25.2"
gene 1..2025
/gene="TMEM40"
/note="transmembrane protein 40"
/db_xref="GeneID:55287"
/db_xref="HGNC:HGNC:25620"
exon 1..69
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:898442973"
variation 6
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:545756764"
variation 8
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:995604096"
variation 10
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:548555777"
variation 12
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461140321"
variation 13
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106623124"
variation 19
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:898157286"
variation 20
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349864418"
variation 22
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226310238"
variation 29
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286149706"
variation 36
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1004647109"
variation 38
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061552390"
variation 39
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:907286199"
variation 40
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1264877009"
variation 45
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061552338"
variation 47
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201005244"
variation 50
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061552306"
variation 52
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456841293"
variation 54
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:111647271"
misc_feature 57..59
/gene="TMEM40"
/note="upstream in-frame stop codon"
variation 57
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061552251"
variation 64
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489884384"
variation 65
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201757082"
exon 70..150
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 70
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:554298828"
variation 72
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1334089670"
variation 74
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:771747873"
variation 75
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:745880701"
variation 76
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:778681912"
variation 77
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756838370"
CDS 78..779
/gene="TMEM40"
/note="isoform b is encoded by transcript variant 2"
/codon_start=1
/product="transmembrane protein 40 isoform b"
/protein_id="NP_060776.2"
/db_xref="CCDS:CCDS2613.1"
/db_xref="GeneID:55287"
/db_xref="HGNC:HGNC:25620"
/translation="
METSASSSQPQDNSQVHRETEDVDYGETDFHKQDGKAGLFSQEQYERNKSSSSSSSSSSSSSSSSSSSSSESNDEDQQPRATGKHRRSLGAGYPHGNGSPGPGHGEPDVLKDELQLYGDAPGEVVPSGESGLRRRGSDPASGEVEASQLRRLNIKKDDEFFHFVLLCFAIGALLVCYHYYADWFMSLGVGLLTFASLETVGIYFGLVYRIHSVLQGFIPLFQKFRLTGFRKTD"
misc_feature 78..506
/gene="TMEM40"
/note="propagated from UniProtKB/Swiss-Prot (Q8WWA1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 78..80
/gene="TMEM40"
/note="N-acetylmethionine.
/evidence=ECO:0000269|PubMed:12665801, ECO:0000269|Ref.6;
propagated from UniProtKB/Swiss-Prot (Q8WWA1.2);
acetylation site"
misc_feature 414..773
/gene="TMEM40"
/note="Transmembrane protein 40 family; Region: TMEM40;
pfam15817"
/db_xref="CDD:464892"
misc_feature 486..488
/gene="TMEM40"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:19367720; propagated from
UniProtKB/Swiss-Prot (Q8WWA1.2); phosphorylation site"
misc_feature 555..617
/gene="TMEM40"
/note="propagated from UniProtKB/Swiss-Prot (Q8WWA1.2);
transmembrane region"
misc_feature 636..698
/gene="TMEM40"
/note="propagated from UniProtKB/Swiss-Prot (Q8WWA1.2);
transmembrane region"
variation 78
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378759603"
variation 79
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061459636"
variation 81
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177576409"
variation 82
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:534045803"
variation 84
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753348848"
variation 85
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061459517"
variation 92
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1237774656"
variation 93..101
/gene="TMEM40"
/replace="tcctcc"
/replace="tcctcctcc"
/db_xref="dbSNP:2061459324"
variation 93
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755760542"
variation 94
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061459413"
variation 95
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:751985921"
variation 97
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376280227"
variation 101
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1181885301"
variation 103
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:763196102"
variation 104
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352316279"
variation 105
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306714694"
variation 106
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765614026"
variation 108
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213676333"
variation 109
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:373195760"
variation 113
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775983882"
variation 116
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283926641"
variation 119
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776628023"
variation 122
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464884197"
variation 123
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061458956"
variation 130
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329112731"
variation 135
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:764317274"
variation 138
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1393426184"
variation 141
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061458839"
variation 142
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307710995"
variation 144
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760949908"
variation 146
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419244728"
variation 147
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775566858"
variation 149
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:771938508"
exon 151..288
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 151
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1575738532"
variation 155
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218597523"
variation 157
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:1316638280"
variation 160
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226187749"
variation 163
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369681331"
variation 165
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754524080"
variation 167
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147231365"
variation 168
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061449487"
variation 169
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292007306"
variation 175
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1559529752"
variation 176
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:757616974"
variation 178
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402221772"
variation 180
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:754379964"
variation 183
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464884208"
variation 186
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421457193"
variation 193
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106615383"
variation 195..198
/gene="TMEM40"
/replace="tt"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1178127321"
variation 197
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195856797"
variation 199
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061449209"
variation 201
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433267756"
variation 202
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:201694243"
variation 207
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:778227306"
variation 211
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189116924"
variation 213
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:146477309"
variation 214
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:752677259"
variation 215
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:199675070"
variation 218..223
/gene="TMEM40"
/replace="aa"
/replace="aaacaa"
/db_xref="dbSNP:2061448619"
variation 219
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456706816"
variation 220
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:759617035"
variation 222
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234524938"
variation 224
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:751793360"
variation 228..253
/gene="TMEM40"
/replace="tcttcctcctc"
/replace="tcttcctcctcctcctcttcctcctc"
/db_xref="dbSNP:772697831"
variation 229
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:766343986"
variation 231..244
/gene="TMEM40"
/replace="tcctcctc"
/replace="tcctcctcctc"
/replace="tcctcctcctcctc"
/db_xref="dbSNP:760060307"
variation 235
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225719565"
variation 236
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:762820198"
variation 237..253
/gene="TMEM40"
/replace="tcctcctcttcctcctc"
/replace="tcctcctcttcctcctcttcctcctc"
/db_xref="dbSNP:1186188920"
variation 238
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:773305871"
variation 239
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:139413903"
variation 241
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:761392282"
variation 242
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061448361"
variation 246..265
/gene="TMEM40"
/replace="tcctcctcatcctcctcatc"
/replace="tcctcctcatcctcctcatcctcctcatc"
/db_xref="dbSNP:1376602587"
variation 247..248
/gene="TMEM40"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2061448298"
variation 250
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:111630194"
variation 251
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061448216"
variation 252..280
/gene="TMEM40"
/replace="tcatcctcctc"
/replace="tcatcctcctcatcttcttcatcctcctc"
/replace="tcatcctcctcatcttcttcatcctcctcatcttcttcatcctcctc"
/db_xref="dbSNP:1212455711"
variation 254
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:768201416"
variation 255..262
/gene="TMEM40"
/replace="tcctc"
/replace="tcctcctc"
/db_xref="dbSNP:1381984783"
variation 257
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:994744830"
variation 259..260
/gene="TMEM40"
/replace="c"
/replace="cc"
/db_xref="dbSNP:746446378"
variation 263
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293946557"
variation 268
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:746709593"
variation 269
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:779654495"
variation 270..274
/gene="TMEM40"
/replace="tc"
/replace="tcatc"
/db_xref="dbSNP:779392279"
variation 272
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771330558"
variation 273..286
/gene="TMEM40"
/replace="tcctcctcctc"
/replace="tcctcctcctcctc"
/replace="tcctcctcctcctcctc"
/db_xref="dbSNP:749687247"
variation 275
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:749603635"
variation 277
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177619740"
variation 280
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106615297"
variation 284
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061447574"
variation 288
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:778280857"
exon 289..378
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 292
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401705781"
variation 293
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:976135454"
variation 299
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:371342903"
variation 305
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296996681"
variation 307
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:759243337"
variation 308
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:773988101"
variation 310..311
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:777818233"
variation 313
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138475655"
variation 314
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:777035977"
variation 317
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1473359782"
variation 318
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:769141454"
variation 320..321
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2061403603"
variation 320
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478410536"
variation 322..323
/gene="TMEM40"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1559527453"
variation 323
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200226147"
variation 324
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:758550120"
variation 330
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:140722236"
variation 332
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453389097"
variation 333
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:150198487"
variation 334
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:151070915"
variation 335
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:923887280"
variation 336
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142209950"
variation 337
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756019404"
variation 338
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:752615328"
variation 339
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061403067"
variation 340
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:767079629"
variation 341
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145273097"
variation 344
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061402930"
variation 345
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:774039474"
variation 346
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332317453"
variation 347
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061402893"
variation 348
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323817467"
variation 350
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061402841"
variation 352
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028812518"
variation 354
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385825502"
variation 355
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:766015200"
variation 356
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:762089697"
variation 357
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:776998006"
variation 360
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423618319"
variation 362
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374102262"
variation 363..365
/gene="TMEM40"
/replace="gg"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2061402596"
variation 363
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:145443570"
variation 367
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:139503455"
variation 368
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:115733141"
variation 369..372
/gene="TMEM40"
/replace=""
/replace="ggct"
/db_xref="dbSNP:2061402457"
variation 369
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:779031190"
variation 373
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:771114844"
variation 374
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061402385"
variation 375
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1559527366"
variation 377
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240228265"
variation 378
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:146365508"
exon 379..432
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 379
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061391943"
variation 383
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751437669"
variation 384
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061391846"
variation 389
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:779680125"
variation 390..393
/gene="TMEM40"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1433016693"
variation 390
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:757813828"
variation 391
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:750136247"
variation 392
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1391680924"
variation 393
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:764930665"
variation 395
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061391565"
variation 396
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1362468360"
variation 398
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061391503"
variation 401
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75917614"
variation 402
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:544710139"
variation 406
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:774718081"
variation 410
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:147051806"
variation 411
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061391344"
variation 413
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1473646979"
variation 416
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:762921329"
variation 417
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446668104"
variation 418
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:369888905"
variation 419
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:769936195"
variation 421
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:747949810"
variation 422
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:147608337"
variation 423
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392339075"
variation 426
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:768433349"
variation 427
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047604956"
variation 430
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:747005245"
variation 431
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380345955"
variation 432
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1575733961"
exon 433..468
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 438
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:760519202"
variation 441
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061356089"
variation 442
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061356063"
variation 445
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:201284102"
variation 446
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376845516"
variation 448
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1303447674"
variation 450
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:143024232"
variation 451
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367231631"
variation 453
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:759461512"
variation 458
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:774401744"
variation 461
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:34632635"
variation 468
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303872903"
exon 469..501
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 469
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219116298"
variation 470
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061352003"
variation 474
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756191439"
variation 475
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:144017136"
variation 478
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:113852939"
variation 483
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061351805"
variation 484
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044795477"
variation 490
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:777040204"
variation 491
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345878507"
variation 492
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:192420814"
variation 493
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:751333865"
variation 496
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354302728"
variation 497
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:201898990"
variation 500
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:763050250"
exon 502..549
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 503
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372524828"
variation 504
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:760390215"
variation 505
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:199973876"
variation 507
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:186695288"
variation 508
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1559524365"
variation 509
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:749619163"
variation 510
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:935284406"
variation 513
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:370097007"
variation 514
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:770270888"
variation 515
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:748191325"
variation 520
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1262893957"
variation 525
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339511174"
variation 527..528
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2061348069"
variation 527
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269040654"
variation 530
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224575860"
variation 533
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:1321915437"
variation 535
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:367768113"
variation 537
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334691432"
variation 538
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:58619724"
variation 542
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:58194358"
variation 543
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:755077473"
variation 544
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:747282610"
variation 546
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:923858021"
variation 547
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1333974661"
variation 549
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410976328"
exon 550..621
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 550
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:552698091"
variation 551
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470355082"
variation 552
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:746059728"
variation 555
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:960173379"
variation 561
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:778831448"
variation 563
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1559523737"
variation 564
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341758"
variation 566
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:759003406"
variation 567
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:201284335"
variation 569
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:777641656"
variation 572
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345326620"
variation 573
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287649219"
variation 575
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368924026"
variation 576
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341599"
variation 578
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:966066812"
variation 582
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:139984617"
variation 583
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:752136985"
variation 585
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1450788139"
variation 585
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:550278148"
variation 587
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356218473"
variation 588
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759291365"
variation 590
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412958493"
variation 592
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450480545"
variation 596
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314961568"
variation 599
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:751168020"
variation 600
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:953462561"
variation 612
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:776220889"
variation 613
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:762034501"
variation 615
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061341161"
variation 617
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:373401700"
variation 618
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760847101"
variation 619
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1418427179"
variation 621
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061341045"
exon 622..696
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 623
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1469130769"
variation 625
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061339983"
variation 627
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164164101"
variation 631
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273179654"
variation 634
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:759490002"
variation 636
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339879"
variation 637
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061339858"
variation 638
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061339842"
variation 642
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:774670198"
variation 644
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:977553907"
variation 645
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:770995861"
variation 646
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:868310575"
variation 648
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339693"
variation 650
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488586319"
variation 651
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360154395"
variation 652
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276765886"
variation 653
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:749095466"
variation 655
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773049502"
variation 657
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325197141"
variation 658
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:879899138"
variation 659
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:199796616"
variation 660
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:911874972"
variation 664
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:748125475"
variation 665
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061339409"
variation 667
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453098809"
variation 674
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:975450770"
variation 675
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416950549"
variation 676
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:530184924"
variation 684
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455019771"
variation 685
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1252734807"
variation 686
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1245647594"
variation 689
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1019610401"
variation 690
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370473375"
variation 693
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756746842"
variation 696
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061339099"
exon 697..759
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 697
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253897426"
variation 698
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573756207"
variation 702
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:142014087"
variation 703
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:778662525"
variation 704
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061331662"
variation 706
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:756581348"
variation 707
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1559522794"
variation 708
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:981186990"
variation 713
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:752942962"
variation 714
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781731021"
variation 715
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061331426"
variation 722
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:755496353"
variation 724
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766488618"
variation 725
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106603947"
variation 729
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188760686"
variation 730
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038019158"
variation 731..735
/gene="TMEM40"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:774951652"
variation 731
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004834801"
variation 732
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:763000143"
variation 734
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422589609"
variation 735
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147042676"
variation 737
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061330989"
variation 741
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046382107"
variation 748
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061330927"
variation 751
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761682115"
variation 752
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310290440"
variation 753
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323328731"
variation 759
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:776346899"
exon 760..2025
/gene="TMEM40"
/inference="alignment:Splign:2.1.0"
variation 761
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:78560646"
variation 765
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1575727833"
variation 766
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:572073706"
variation 768
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333571568"
variation 770..779
/gene="TMEM40"
/replace="gactga"
/replace="gactgactga"
/db_xref="dbSNP:771597719"
variation 774
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752057963"
variation 775
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228908752"
variation 782
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:555363314"
variation 784
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543359174"
variation 785
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:750443698"
variation 788
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:974451187"
variation 790
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061326186"
variation 791
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061326166"
variation 792
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461347275"
variation 793
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:749797798"
variation 794
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061326110"
variation 795
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236830117"
variation 796
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972914916"
variation 800
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:961590176"
variation 802
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462505977"
variation 805
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:370226089"
variation 811
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:762003898"
variation 812
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:754055798"
variation 814
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:763841790"
variation 815
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193984555"
variation 816
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1575727769"
variation 818
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:1559522311"
variation 818
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061325859"
variation 819
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430587953"
variation 824
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760466277"
variation 825
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287571324"
variation 827
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197041325"
variation 828
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:11549481"
variation 830
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:187016181"
variation 831
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325718"
variation 833..836
/gene="TMEM40"
/replace="cc"
/replace="cccc"
/db_xref="dbSNP:2061325646"
variation 834
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325707"
variation 835
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281401864"
variation 836
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061325614"
variation 841
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325591"
variation 843
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:373781796"
variation 844
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1376619076"
variation 845
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106603251"
variation 848
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:908947237"
variation 849
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325505"
variation 850
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419424093"
variation 851
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005668509"
variation 855
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325430"
variation 859
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1207397049"
variation 862
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061325382"
variation 871
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:895219593"
variation 872
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382479847"
variation 873
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061325307"
variation 876
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328805489"
variation 881
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061325266"
variation 883
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235878772"
variation 886
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1559522262"
variation 887
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:950546894"
variation 889
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:557354496"
variation 892
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061325139"
regulatory 894..899
/regulatory_class="polyA_signal_sequence"
/gene="TMEM40"
/note="hexamer: AATAAA"
variation 899
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603194"
variation 901
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:1352903966"
variation 901
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325077"
variation 902
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061325043"
variation 905
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214172689"
variation 906
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1024774414"
variation 908
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324962"
variation 912
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061324930"
polyA_site 918
/gene="TMEM40"
/note="major polyA site"
variation 921
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:184140764"
variation 923
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324895"
variation 924..926
/gene="TMEM40"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:2061324871"
variation 931
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033645097"
variation 932
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205988113"
variation 935
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324816"
variation 937
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603141"
variation 940
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324793"
variation 944
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221154942"
variation 945
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452608250"
variation 948
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195596186"
variation 949
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106603125"
variation 951
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1396146687"
variation 952
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:959301594"
variation 959
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061324659"
variation 967
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324642"
variation 969
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:780495165"
variation 972
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061324616"
variation 973
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061324600"
variation 976
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157342573"
variation 979
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:571742502"
variation 983
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1034068547"
variation 989
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000861742"
variation 990
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1003465624"
variation 991
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:557830885"
variation 992
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045602569"
variation 996
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:945938402"
variation 998
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442380720"
variation 999
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061324427"
variation 1000..1001
/gene="TMEM40"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2061324407"
variation 1003
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1575727623"
variation 1004
/gene="TMEM40"
/replace="c"
/replace="cctc"
/db_xref="dbSNP:1009687494"
variation 1007
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:2061324337"
variation 1009
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1376043722"
variation 1013
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1559522192"
variation 1014
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237933502"
variation 1015
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061324259"
variation 1018..1021
/gene="TMEM40"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:891266065"
variation 1019
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324240"
variation 1020
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1308841891"
variation 1028
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061324180"
variation 1029
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243831377"
variation 1032..1035
/gene="TMEM40"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:1467318551"
variation 1035
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:191951760"
variation 1040
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1215617283"
variation 1043
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:932864291"
variation 1045
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054690212"
variation 1050
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323968"
variation 1052
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039052998"
variation 1055
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419981592"
variation 1061
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:769316546"
variation 1066
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415193203"
variation 1068
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462750727"
variation 1073
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:565749503"
variation 1076
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061323845"
variation 1079
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:908906225"
variation 1086
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344078949"
variation 1087
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323795"
variation 1091
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:143263158"
variation 1094
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323768"
variation 1095
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299772836"
variation 1100
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323725"
variation 1105
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323714"
variation 1106
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323695"
variation 1112
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373970379"
variation 1113
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323664"
variation 1114
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323619"
variation 1119
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:763965908"
variation 1119
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395176903"
variation 1120
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323569"
variation 1122
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:929062423"
variation 1126
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323532"
variation 1130
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415788974"
variation 1138
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323501"
variation 1142
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:529252664"
variation 1146
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1317334783"
variation 1147
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323445"
variation 1149
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392931789"
variation 1151
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323399"
variation 1153
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:917726590"
variation 1155
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602915"
variation 1156
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:758190414"
variation 1157
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061323353"
variation 1159
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181636886"
variation 1160
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:560203523"
variation 1162
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:922245044"
variation 1163
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:149560856"
variation 1165
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422510477"
variation 1170
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061323196"
variation 1171
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1407645934"
variation 1173
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1575727508"
variation 1174
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:780747504"
variation 1178
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171918400"
variation 1179
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:547822092"
variation 1181
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:984657318"
variation 1186..1187
/gene="TMEM40"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2061323033"
variation 1186
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061323059"
variation 1187
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:926543031"
variation 1189..1191
/gene="TMEM40"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2061322965"
variation 1190
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959456134"
variation 1191
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:968067857"
variation 1195
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212868549"
variation 1197
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322917"
variation 1200
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033696155"
variation 1202
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602865"
variation 1203..1210
/gene="TMEM40"
/replace="g"
/replace="gtccactg"
/db_xref="dbSNP:1210092586"
variation 1205
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602861"
variation 1206
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061322867"
variation 1207
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322852"
variation 1209
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1317715882"
variation 1210
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279830733"
variation 1215
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1009615712"
variation 1217
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:756928391"
variation 1218
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061322745"
variation 1226
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229412617"
variation 1228
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955457370"
variation 1230
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:765132159"
variation 1231
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187756958"
variation 1233
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061322641"
variation 1234
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602819"
variation 1239
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212731913"
variation 1240
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1361234908"
variation 1241
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432119914"
variation 1246
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1029805112"
variation 1247
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377205179"
variation 1248
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:906569375"
variation 1249
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:73022960"
variation 1252
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061322480"
variation 1258
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322461"
variation 1266
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322445"
variation 1267
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:777725325"
variation 1269
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533201631"
variation 1274
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061322392"
variation 1275
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564227282"
variation 1276
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061322351"
variation 1277
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322324"
variation 1278
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2106602762"
variation 1283
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322310"
variation 1284
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061322288"
variation 1285..1286
/gene="TMEM40"
/replace=""
/replace="c"
/db_xref="dbSNP:1449519344"
variation 1285
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:2061322120"
variation 1285
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010189712"
variation 1286..1293
/gene="TMEM40"
/replace="ttttttt"
/replace="tttttttt"
/replace="ttttttttt"
/db_xref="dbSNP:1233697830"
variation 1286
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061322027"
variation 1287
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1428936263"
variation 1289
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:900020982"
variation 1293
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321950"
variation 1295
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:758201843"
variation 1297
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006226627"
variation 1299
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061321873"
variation 1300..1308
/gene="TMEM40"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/replace="aaaaaaaaaa"
/db_xref="dbSNP:571290515"
variation 1300
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054302206"
variation 1304
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047406760"
variation 1305
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1559521994"
variation 1306
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1168831260"
variation 1308
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321736"
variation 1309..1310
/gene="TMEM40"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1487836902"
variation 1309
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2106602693"
variation 1310
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1559521975"
variation 1311
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321687"
variation 1313
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:917653039"
variation 1320
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396800309"
variation 1323
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428422583"
variation 1327..1336
/gene="TMEM40"
/replace=""
/replace="agaaactaaa"
/db_xref="dbSNP:1559521952"
variation 1328
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1559521958"
variation 1331
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454709670"
variation 1332
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935802110"
variation 1336
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415099851"
variation 1337
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056166540"
variation 1338
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321528"
variation 1339
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:889555568"
variation 1340
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727366"
variation 1341
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484692269"
variation 1344
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321452"
variation 1347
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256910426"
variation 1348
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321397"
variation 1349
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324031836"
variation 1350
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321368"
variation 1351
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373817976"
variation 1352
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061321310"
variation 1354
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061321281"
variation 1355
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061321265"
variation 1357
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321238"
variation 1358
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049528363"
variation 1359
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:186721457"
variation 1364
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602607"
variation 1365
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602604"
variation 1369
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:922295826"
variation 1371
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:527348786"
variation 1373
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565286019"
variation 1374
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:940288964"
variation 1375
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333778835"
variation 1380
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211274247"
variation 1386
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061321047"
variation 1387
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061321028"
variation 1390
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254380179"
variation 1398
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:543891434"
variation 1400
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320968"
variation 1401
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177879766"
variation 1402
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561743747"
variation 1403
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313260472"
variation 1404
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320883"
variation 1410
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320867"
variation 1412
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:913879963"
variation 1415
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776127551"
variation 1418
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:182996297"
variation 1422
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061320772"
variation 1426
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320762"
variation 1427
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:955385950"
variation 1428..1429
/gene="TMEM40"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2061320710"
variation 1431
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353008754"
variation 1433
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061320608"
variation 1434
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106602517"
variation 1435
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162839130"
variation 1437
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396838472"
variation 1438
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1441758196"
variation 1441
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:575937892"
variation 1446
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328699630"
variation 1447..1451
/gene="TMEM40"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:2061320479"
variation 1448
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320500"
variation 1451
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061320457"
variation 1452
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1334526865"
variation 1453
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444801147"
variation 1454
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410027438"
variation 1455
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372079483"
variation 1456
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:191855001"
variation 1461
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061320322"
variation 1462..1470
/gene="TMEM40"
/replace="tttttttt"
/replace="ttttttttt"
/replace="tttttttttt"
/db_xref="dbSNP:531847151"
variation 1470
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:982192029"
variation 1474
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061320259"
variation 1476
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334877087"
variation 1479
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320231"
variation 1480
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061320214"
variation 1483
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:561509065"
variation 1484..1485
/gene="TMEM40"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1270725312"
variation 1485
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:970779301"
variation 1486
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020995949"
variation 1487
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:138496707"
variation 1488..1508
/gene="TMEM40"
/replace="gtacatacctg"
/replace="gtacatacctgtacatacctg"
/db_xref="dbSNP:2061319859"
variation 1488
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061320105"
variation 1489
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256587958"
variation 1491
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:964211486"
variation 1492
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:955994532"
variation 1494
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575727243"
variation 1496
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061320018"
variation 1497
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319997"
variation 1500
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017525322"
variation 1501
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319962"
variation 1502
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319934"
variation 1503
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033316141"
variation 1504
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1394966644"
variation 1505
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167451441"
variation 1509
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329939972"
variation 1510
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:577823696"
variation 1518
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360940403"
variation 1520
/gene="TMEM40"
/replace=""
/replace="a"
/db_xref="dbSNP:1417239478"
variation 1521
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355712069"
variation 1523
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319664"
variation 1525
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183035746"
variation 1530
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319609"
variation 1535
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:368027790"
variation 1541
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:557894404"
variation 1542
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1196357619"
variation 1543
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049581794"
variation 1544
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047331885"
variation 1545
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727209"
variation 1548
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319463"
variation 1549
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319447"
variation 1550
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061319436"
variation 1552
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1484542768"
variation 1555
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:997973118"
variation 1560
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:900885350"
variation 1565
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036709497"
variation 1570
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259862199"
variation 1573
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:939654196"
variation 1578
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061319299"
variation 1581
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192524021"
variation 1582
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480155561"
variation 1584
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1371459537"
variation 1589
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319222"
variation 1590
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319205"
variation 1591
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319185"
variation 1594
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265870515"
variation 1598
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727178"
variation 1600
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215482393"
variation 1601
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:201820100"
variation 1603
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061319092"
variation 1607
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:910154428"
variation 1609
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:111300148"
variation 1610
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:938255041"
variation 1612
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061319011"
variation 1613
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318994"
variation 1616
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318979"
variation 1617
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:374274432"
variation 1618
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375671511"
variation 1623
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318932"
variation 1624
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4684873"
variation 1627
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304327322"
variation 1631
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1368726760"
variation 1633
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302519316"
variation 1636..1637
/gene="TMEM40"
/replace=""
/replace="tt"
/db_xref="dbSNP:1460309668"
variation 1636..1637
/gene="TMEM40"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1280835299"
variation 1636
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:79636268"
variation 1637..1639
/gene="TMEM40"
/replace=""
/replace="taa"
/db_xref="dbSNP:2106602292"
variation 1637..1638
/gene="TMEM40"
/replace=""
/replace="ta"
/db_xref="dbSNP:1394457233"
variation 1637
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1295719667"
variation 1638..1653
/gene="TMEM40"
/replace="aaaaaaaaaaa"
/replace="aaaaaaaaaaaa"
/replace="aaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaa"
/db_xref="dbSNP:rs371416811"
variation 1638
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:75135909"
variation 1639
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:368364111"
variation 1642
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318623"
variation 1648..1649
/gene="TMEM40"
/replace=""
/replace="g"
/db_xref="dbSNP:2061318602"
variation 1650
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318586"
variation 1652
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318569"
variation 1653..1661
/gene="TMEM40"
/replace="a"
/replace="agacaaata"
/db_xref="dbSNP:2061318339"
variation 1654
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1575727122"
variation 1655
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318437"
variation 1656
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575727119"
variation 1657..1663
/gene="TMEM40"
/replace="aaa"
/replace="aaataaa"
/db_xref="dbSNP:1175883619"
variation 1657..1659
/gene="TMEM40"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1160580651"
variation 1660
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453186639"
variation 1661
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602238"
variation 1665
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318300"
variation 1668
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061318284"
variation 1670
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378622935"
variation 1672
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171051062"
variation 1675
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318218"
variation 1677
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458849275"
variation 1682
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061318184"
variation 1683
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1453521549"
variation 1684
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286712883"
variation 1685
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:937765087"
variation 1687
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061318019"
variation 1690
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:926828928"
variation 1692
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:904986395"
variation 1695
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317963"
variation 1697
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317946"
variation 1701
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061317931"
variation 1703
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368663796"
variation 1707
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061317890"
variation 1710
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181348334"
variation 1714
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304099712"
variation 1715
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1316076473"
variation 1718
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1434050554"
variation 1719
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043969277"
variation 1723
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259124259"
variation 1724
/gene="TMEM40"
/replace=""
/replace="t"
/db_xref="dbSNP:2061317745"
variation 1727
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575727057"
variation 1730
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317711"
variation 1731
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317691"
variation 1732..1735
/gene="TMEM40"
/replace="at"
/replace="atat"
/db_xref="dbSNP:2061317638"
variation 1732
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353180640"
variation 1733
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:982244380"
variation 1735
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:970792316"
variation 1736
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:913804721"
variation 1740..1742
/gene="TMEM40"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2106602166"
variation 1746
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:988079636"
variation 1750
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:555427769"
variation 1752
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:750488799"
variation 1755
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:913944643"
variation 1756
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418792913"
variation 1757
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1575727031"
variation 1762
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317451"
variation 1765
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:922607566"
variation 1770
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317416"
variation 1776
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061317382"
variation 1779
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:988175450"
variation 1780
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272434166"
variation 1784
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113231678"
variation 1787
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:7626048"
variation 1788
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462592681"
variation 1790
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317231"
variation 1791
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1000147868"
variation 1795
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317196"
variation 1798
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1372544367"
variation 1799
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:879463121"
variation 1802
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061317145"
variation 1803
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:953940518"
variation 1810
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061317103"
variation 1812
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237868039"
variation 1815
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317075"
variation 1817
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061317057"
variation 1818
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312447007"
variation 1823
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061317020"
variation 1825
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1306055461"
variation 1826
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316971"
variation 1827
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439097537"
variation 1833
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229295581"
variation 1834
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017076554"
variation 1835
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370756899"
variation 1839
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:369561840"
variation 1841
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106602090"
variation 1844
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316834"
variation 1845
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437975459"
variation 1848
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:2061316768"
variation 1851
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316750"
variation 1853
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316727"
variation 1854
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316714"
variation 1857
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478672208"
variation 1858
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316681"
variation 1868
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1382878591"
variation 1871
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:1175819973"
variation 1874
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2106602064"
variation 1877..1878
/gene="TMEM40"
/replace="g"
/replace="gg"
/db_xref="dbSNP:549728818"
variation 1878
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253170755"
variation 1881
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186731337"
variation 1882
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415219866"
variation 1883
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028162612"
variation 1887
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164931337"
variation 1893
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353852173"
variation 1900
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:997986150"
variation 1904
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:2061316474"
variation 1906
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316452"
variation 1909
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460439460"
variation 1914
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316426"
variation 1915
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1379543055"
variation 1929
/gene="TMEM40"
/replace="a"
/replace="c"
/db_xref="dbSNP:900934953"
variation 1930
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172045703"
variation 1931
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316348"
variation 1933
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316335"
variation 1939
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452271734"
variation 1941
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037164895"
variation 1943
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014495352"
variation 1945
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:2061316250"
variation 1951
/gene="TMEM40"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003948212"
variation 1957
/gene="TMEM40"
/replace="g"
/replace="t"
/db_xref="dbSNP:896120426"
variation 1960
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:888141067"
variation 1961
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048053338"
variation 1966
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253628195"
variation 1967
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:2061316116"
variation 1968
/gene="TMEM40"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2061316096"
variation 1969
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:938307308"
variation 1972
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316060"
variation 1978
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316041"
variation 1979
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2061316025"
variation 1985
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:905415695"
variation 1987
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046560537"
variation 1997
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:949531026"
variation 1998
/gene="TMEM40"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180890994"
variation 1999
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:904953560"
regulatory 2003..2008
/regulatory_class="polyA_signal_sequence"
/gene="TMEM40"
/note="hexamer: AATAAA"
variation 2009
/gene="TMEM40"
/replace="a"
/replace="g"
/db_xref="dbSNP:2106601989"
variation 2012
/gene="TMEM40"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259015025"
variation 2021
/gene="TMEM40"
/replace="c"
/replace="t"
/db_xref="dbSNP:377712522"
variation 2022
/gene="TMEM40"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:550052209"
polyA_site 2025
/gene="TMEM40"
/note="major polyA site"
ORIGIN
gaccagcccagcatccacatagtctacacagagctccccttgctgcccagacaagctgaaggaccacaggaaaagccatggagacttcagcatcctcctcccagcctcaggacaacagtcaagtccacagagaaacagaagatgtagactatggagagacagatttccacaagcaagatgggaaggctggactcttttcccaagaacaatatgagagaaacaagtcttcttcctcctcctcctcttcctcctcatcctcctcatcttcttcatcctcctcctcctcagagagcaatgatgaggaccagcaacccagagcaaccggaaaacatcgacggagcctgggggctggatacccccacgggaacggctcacccggtcctgggcatggggagcctgacgttttgaaggatgagcttcaactctatggagatgctcctggagaggtggtaccctctggggaatcaggactccgaaggagaggctctgacccagcaagtggagaagtggaggcctctcagttaagaagactgaatataaagaaagatgatgagtttttccatttcgtcctcctgtgctttgccatcggggccttgctggtgtgttatcactattacgcagactggttcatgtctcttggggtcggcctgctcaccttcgcctccctggaaaccgttggcatctacttcggactagtgtaccgtatccacagcgtcctccaaggcttcatccccctcttccagaagtttaggctgacagggttcaggaagactgactgaggccacttccaggtgggcagcagaggcaggccccagtgtgaccaccactgcgacccctgagcccacaagggcagagcagcattctgagagacgcacaggagaccaagccagaccaataaacagaacacttttccttccatgtggtctgaatgttggcaccagcccgggcaggggcatctcatttgggcagtactgctgtgcaacccagctgcaaggatggaaggcagagggtgggtgtggggcctgaggcttcacagtacctggaccagcaggaagattctgggaggtcactgctctcagaggacagcaagggaccctgagctctgcaagctgtgatctgtctgggttcatggtttttctcaaatcccaggctatctgcatgcgctctcaggtgctaccgagccatcctgggagagatggatggtccactgctttgaggcagggagccatcgggctggggccccttggtgaacctgatgcaggtaagatgctgaggactaaaaccattttttttgcacccaaaaaaaaaggcaggaaaatgatcatcagaaactaaatggcagccaggcatgggggctcacaactgtaatcctcgcactttgggaggctcaggctaagggtcgcttgaagctgagagttcaagaccaacctgggcaacatagtgagacccccatctctacaatttttttttaatgaccaaatgtggcggtacatacctgtacatacctgcggttccagctactcaagaggctgaggcaggaggactgcttgagcccaggagttcagggctgcagtgaggtacgatcaagccactgcactccagcctgggcgacagagcaagatcgtttctctaaaattaaaaaaaaaaaaaaaagacaaataaaaattgcatgtatttgtagtgtacaacatgttttgaaatatgtggaatggctaaatcaagctaattaacatatgtatccctcacataccctttttttatgatgagaacagtaaaaacctactgtcagcaatttgcaaagtatacaatacattgttattaactatggtcaccatgctatgtgattgatatcctgaacttgaactgagttcttgatggtcacagacatgctgttctcaaaactcagaagggtaacttctgaggttttgatttcaagtacttgtatgtaacctaatttaacgggagcccagagtgcacagatcagatatttattaaacatataaataaaacacagttttcacgata
//
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.
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