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2025-05-09 16:28:53, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_032167 8172 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens sorting nexin 29 (SNX29), mRNA.
ACCESSION NM_032167
VERSION NM_032167.3 GI:343780937
KEYWORDS RefSeq.
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 8172)
AUTHORS Borglum AD, Demontis D, Grove J, Pallesen J, Hollegaard MV,
Pedersen CB, Hedemand A, Mattheisen M, Uitterlinden A, Nyegaard M,
Orntoft T, Wiuf C, Didriksen M, Nordentoft M, Nothen MM, Rietschel
M, Ophoff RA, Cichon S, Yolken RH, Hougaard DM, Mortensen PB and
Mors O.
CONSRTM GROUP investigators
TITLE Genome-wide study of association and interaction with maternal
cytomegalovirus infection suggests new schizophrenia loci
JOURNAL Mol. Psychiatry (2013) In press
PUBMED 23358160
REMARK Publication Status: Available-Online prior to print
REFERENCE 2 (bases 1 to 8172)
AUTHORS Comuzzie,A.G., Cole,S.A., Laston,S.L., Voruganti,V.S., Haack,K.,
Gibbs,R.A. and Butte,N.F.
TITLE Novel genetic loci identified for the pathophysiology of childhood
obesity in the Hispanic population
JOURNAL PLoS ONE 7 (12), E51954 (2012)
PUBMED 23251661
REFERENCE 3 (bases 1 to 8172)
AUTHORS Fox CS, Liu Y, White CC, Feitosa M, Smith AV, Heard-Costa N, Lohman
K, Johnson AD, Foster MC, Greenawalt DM, Griffin P, Ding J, Newman
AB, Tylavsky F, Miljkovic I, Kritchevsky SB, Launer L, Garcia M,
Eiriksdottir G, Carr JJ, Gudnason V, Harris TB, Cupples LA and
Borecki IB.
CONSRTM GIANT Consortium; MAGIC Consortium; GLGC Consortium
TITLE Genome-wide association for abdominal subcutaneous and visceral
adipose reveals a novel locus for visceral fat in women
JOURNAL PLoS Genet. 8 (5), E1002695 (2012)
PUBMED 22589738
REFERENCE 4 (bases 1 to 8172)
AUTHORS Hosgood,H.D. III, Zhang,L., Shen,M., Berndt,S.I., Vermeulen,R.,
Li,G., Yin,S., Yeager,M., Yuenger,J., Rothman,N., Chanock,S.,
Smith,M. and Lan,Q.
TITLE Association between genetic variants in VEGF, ERCC3 and
occupational benzene haematotoxicity
JOURNAL Occup Environ Med 66 (12), 848-853 (2009)
PUBMED 19773279
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 8172)
AUTHORS Seet,L.F. and Hong,W.
TITLE The Phox (PX) domain proteins and membrane traffic
JOURNAL Biochim. Biophys. Acta 1761 (8), 878-896 (2006)
PUBMED 16782399
REMARK Review article
REFERENCE 6 (bases 1 to 8172)
AUTHORS Loftus,B.J., Kim,U.J., Sneddon,V.P., Kalush,F., Brandon,R.,
Fuhrmann,J., Mason,T., Crosby,M.L., Barnstead,M., Cronin,L.,
Deslattes Mays,A., Cao,Y., Xu,R.X., Kang,H.L., Mitchell,S.,
Eichler,E.E., Harris,P.C., Venter,J.C. and Adams,M.D.
TITLE Genome duplications and other features in 12 Mb of DNA sequence
from human chromosome 16p and 16q
JOURNAL Genomics 60 (3), 295-308 (1999)
PUBMED 10493829
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AL135642.1, AI369689.1, AC007601.7, BM692924.1, AK074072.1,
AC010333.7 and AL137333.1.
On Aug 17, 2011 this sequence version replaced gi:116292169.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. There are no full-length human
transcripts representing this exon combination; it is predicted
based on tiled partial human transcript alignments and on
full-length orthologous alignments from cow GeneID:518366.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns ERS025081,
ERS025084 [ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
inferred exon combination :: based on alignments, homology
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-397 AL135642.1 1-397
398-836 AI369689.1 1-439 c
837-1161 AC007601.7 122467-122791 c
1162-1360 BM692924.1 1-199
1361-1361 AC007601.7 105552-105552 c
1362-1382 BM692924.1 201-221
1383-2925 AK074072.1 1-1543
2926-7926 AC010333.7 134353-139353 c
7927-8172 AL137333.1 1392-1637
FEATURES Location/Qualifiers
source 1..8172
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16p13.13-p13.12"
gene 1..8172
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/note="sorting nexin 29"
/db_xref="GeneID:92017"
/db_xref="HGNC:30542"
exon 1..69
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
CDS 63..2504
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/note="RUN domain containing 2A; RUN domain-containing
protein 2A"
/codon_start=1
/product="sorting nexin-29"
/protein_id="NP_115543.3"
/db_xref="GI:343780938"
/db_xref="CCDS:CCDS10553.2"
/db_xref="GeneID:92017"
/db_xref="HGNC:30542"
/translation="
MSGSQNNDKRQFLLERLLDAVKQCQIRFGGRKEIASDSDSRVTCLCAQFEAVLQHGLKRSRGLALTAAAIKQAAGFASKTETEPVFWYYVKEVLNKHELQRFYSLRHIASDVGRGRAWLRCALNEHSLERYLHMLLADRCRLSTFYEDWSFVMDEERSSMLPTMAAGLNSILFAINIDNKDLNGQSKFAPTVSDLLKESTQNVTSLLKESTQGVSSLFREITASSAVSILIKPEQETDPLPVVSRNVSADAKCKKERKKKKKVTNIISFDDEEDEQNSGDVFKKTPGAGESSEDNSDRSSVNIMSAFESPFGPNSNGSQSSNSWKIDSLSLNGEFGYQKLDVKSIDDEDVDENEDDVYGNSSGRKHRGHSESPEKPLEGNTCLSQMHSWAPLKVLHNDSDILFPVSGVGSYSPADAPLGSLENGTGPEDHVLPDPGLRYSVEASSPGHGSPLSSLLPSASVPESMTISELRQATVAMMNRKDELEEENRSLRNLLDGEMEHSAALRQEVDTLKRKVAEQEERQGMKVQALARENEVLKVQLKKYVGAVQMLKREGQTAEVPNLWSVDGEVTVAEQKPGEIAEELASSYERKLIEVAEMHGELIEFNERLHRALVAKEALVSQMRQELIDLRGPVPGDLSQTSEDQSLSDFEISNRALINVWIPSVFLRGKAANAFHVYQVYIRIKDDEWNIYRRYTEFRSLHHKLQNKYPQVRAYNFPPKKAIGNKDAKFVEERRKQLQNYLRSVMNKVIQMVPEFAASPKKETLIQLMPFFVDITPPGEPVNSRPKAASRFPKLSRGQPRETRNVEPQSGDL
"
misc_feature 192..599
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/note="RUN domain; Region: RUN; pfam02759"
/db_xref="CDD:190411"
misc_feature 2034..2387
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/note="The phosphoinositide binding Phox Homology domain
of uncharacterized proteins containing PX and RUN domains;
Region: PX_RUN; cd07277"
/db_xref="CDD:132810"
misc_feature order(2142..2150,2220..2225,2262..2264)
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/note="phosphoinositide binding site [chemical binding];
other site"
/db_xref="CDD:132810"
exon 70..131
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
exon 132..184
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 164
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202171381"
variation 170
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:181955535"
exon 185..309
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 215
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:149252396"
variation 218
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372472396"
variation 263
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:144440846"
variation 268
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377206592"
variation 284
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370004640"
variation 303
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375103773"
exon 310..490
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 315
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:181137286"
variation 330
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192074"
variation 347
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:368120914"
variation 353
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:148440564"
variation 356
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:141662337"
variation 387
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200498279"
variation 391
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:146124375"
variation 392
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:75789141"
variation 395
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371965178"
variation 409
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199909749"
variation 434
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376607001"
variation 443
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369593146"
variation 462
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:140116030"
variation 477
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143780467"
exon 491..561
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 494
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:199550971"
variation 537
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146886371"
exon 562..810
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 568
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:200133053"
variation 600
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:139407156"
variation 611
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:150237057"
variation 619
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374491543"
variation 622
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368053179"
variation 629
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:145153392"
variation 647
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:200858924"
variation 650
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3743594"
variation 653
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371953447"
variation 675..677
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gga"
/db_xref="dbSNP:3975443"
variation 687
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:201763407"
variation 698
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3743595"
variation 717..718
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="g"
/db_xref="dbSNP:35545885"
variation 719
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:149165552"
variation 741
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:143274296"
variation 759
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:200913179"
variation 773
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147618832"
variation 785
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3975442"
variation 797
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372474721"
variation 803
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:36013478"
exon 811..1186
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 811
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200420200"
variation 831
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:372445217"
variation 862
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:266788"
variation 898
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:118191509"
variation 902
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:138978522"
variation 914
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:140388401"
variation 915
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:150300274"
variation 920
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375555790"
variation 927
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:200592730"
variation 933
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:79049816"
variation 939
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:698064"
variation 939
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:55983624"
variation 949
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375429695"
variation 950
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:71227598"
variation 950
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147906382"
variation 951
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:149490127"
variation 954
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:201929276"
variation 955
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:266789"
variation 956
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:145959708"
variation 975
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:138572412"
variation 977
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:148525738"
variation 978
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146360621"
variation 980
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:148587635"
variation 995
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142950576"
variation 1004
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:150620705"
variation 1009
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376027540"
variation 1029
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373372248"
variation 1047
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369466275"
variation 1048
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ct"
/db_xref="dbSNP:59755255"
variation 1055
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:373229129"
variation 1057
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:144601555"
variation 1058
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376418962"
variation 1060
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:371644200"
variation 1094
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202120990"
variation 1099
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:374605253"
variation 1103
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147911197"
variation 1109
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376884349"
variation 1130
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142820688"
variation 1167
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:201155615"
variation 1172
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:145545344"
variation 1178
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368090157"
exon 1187..1305
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1187
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:4780409"
variation 1189
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377656568"
variation 1242
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:192392151"
variation 1247
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371077185"
variation 1284
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:375700110"
exon 1306..1381
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1316
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:183275123"
variation 1326
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:188835565"
variation 1331
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373111227"
variation 1336
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:151208037"
variation 1352
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369057566"
variation 1360
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377646847"
variation 1361
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1641843"
variation 1379
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373375033"
exon 1382..1464
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1398
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:201653748"
variation 1404
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373591038"
variation 1460
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:367728075"
exon 1465..1528
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1473
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372788283"
variation 1475
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376551482"
exon 1529..1657
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1532
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199859557"
variation 1547
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:111474722"
variation 1550
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371383536"
variation 1551
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373558970"
variation 1571
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:77098367"
variation 1572
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:188630489"
variation 1573
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:201891583"
variation 1574
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:367917590"
variation 1598
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371866495"
variation 1626
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370517062"
variation 1627
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375035480"
variation 1649
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:368482101"
variation 1652
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372729626"
variation 1655
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:201093247"
exon 1658..1740
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1705
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369323258"
variation 1730
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142571390"
exon 1741..1844
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1775
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201272095"
variation 1823
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200716622"
variation 1826
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:16959111"
variation 1841
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371061201"
exon 1845..1961
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1862
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142589090"
variation 1879
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:144110594"
variation 1885
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375172855"
variation 1915
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369711750"
variation 1919
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:373529545"
variation 1920
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376804586"
variation 1946
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:376970358"
variation 1959
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200035654"
variation 1961
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200955496"
exon 1962..2017
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 1984
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200581572"
variation 1985
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370310558"
exon 2018..2099
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 2039
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:367875213"
variation 2064
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374473805"
variation 2082
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:79448621"
variation 2090
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:368460786"
variation 2091
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:372710575"
exon 2100..2240
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 2120
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376588732"
variation 2132
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369057640"
variation 2138
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373947924"
variation 2174
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:200504324"
exon 2241..2380
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 2280
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:74739074"
variation 2324
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202000492"
variation 2325
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368531765"
variation 2335
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:372832270"
variation 2342
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:190350914"
variation 2350
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376551622"
variation 2369
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:369000584"
variation 2376
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376927002"
variation 2378
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369501793"
exon 2381..8164
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/inference="alignment:Splign:1.39.8"
variation 2391
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:138093631"
variation 2392
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374169541"
variation 2393
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200226941"
variation 2397
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376253899"
variation 2402
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:116521942"
variation 2403
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:200511408"
variation 2409
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:371506902"
variation 2413
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:192670414"
variation 2415
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:75144127"
variation 2416
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201373185"
variation 2418
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:200308141"
variation 2433
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201318041"
variation 2438
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2288423"
variation 2446
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:376360576"
variation 2447
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369902479"
variation 2452
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199674908"
variation 2463
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:202238833"
variation 2466
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:143372184"
variation 2468
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376234366"
variation 2471
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374983257"
variation 2473
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371075864"
variation 2474
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375718452"
variation 2478
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368457017"
variation 2487
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372761841"
variation 2493
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373665690"
variation 2498
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:184647146"
variation 2499
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371635503"
variation 2505
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:369269793"
variation 2508
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376240516"
variation 2509
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:373373575"
variation 2517
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:375169461"
variation 2518
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370216586"
variation 2525
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:190352481"
variation 2526
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376169140"
variation 2530
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2288424"
variation 2533
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372827294"
variation 2536
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377123054"
variation 2537
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201330488"
variation 2547
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373991486"
variation 2550
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377679412"
variation 2551
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:76663189"
variation 2559
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:79920670"
variation 2570
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:181563696"
variation 2573
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2288425"
variation 2578
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:186619116"
variation 2584
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:377483299"
variation 2589
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:189403883"
variation 2593
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138703301"
variation 2600
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370570651"
variation 2601..2602
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:200494454"
variation 2601
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:180884841"
variation 2604..2605
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="ac"
/replace="ca"
/db_xref="dbSNP:71378365"
variation 2604
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1075844"
variation 2605
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:201914201"
variation 2605
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:890897"
variation 2610
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:4997404"
variation 2615
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:5815700"
variation 2615
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142743802"
variation 2626
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:74013306"
variation 2627
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:183513916"
variation 2633
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:186354905"
variation 2636
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270703"
variation 2638
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:28416666"
variation 2652
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:2288427"
variation 2654
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:111875148"
variation 2674
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:201410985"
variation 2685
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:191952671"
variation 2688
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:183274720"
variation 2706
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142424869"
variation 2726
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:371877974"
variation 2743
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:75266351"
variation 2744
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:150893336"
variation 2750
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:139423066"
variation 2781
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374524871"
variation 2791
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1075842"
variation 2794
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1075843"
variation 2800
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375171048"
variation 2809
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144185105"
variation 2840
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:146543361"
variation 2841
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:141249525"
variation 2844
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:77505804"
variation 2872
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143693192"
variation 2874
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:145783090"
variation 2893
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371742377"
variation 2915
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:890896"
variation 2916
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:114748159"
variation 2930
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:116984143"
variation 2934
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148866339"
variation 2946
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2081896"
variation 2968
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374362534"
variation 2996..3001
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gcggggg"
/db_xref="dbSNP:71982769"
variation 2996..3000
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gcgggg"
/db_xref="dbSNP:372417017"
variation 2996
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:201978172"
variation 2997
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:140553943"
variation 2997
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:28571060"
variation 2998
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gggggg"
/db_xref="dbSNP:3074248"
variation 3004
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="cgggg"
/replace="cggggg"
/replace="cggggggg"
/db_xref="dbSNP:60456616"
variation 3005
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="g"
/db_xref="dbSNP:72278291"
variation 3014
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:75211621"
variation 3015
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:61012001"
variation 3078
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369931387"
variation 3081
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:143553329"
variation 3101
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:116430825"
variation 3119
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:188284002"
variation 3135
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:148052852"
variation 3164
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373684333"
variation 3177
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:192799649"
variation 3195
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374073878"
variation 3205
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:182499910"
variation 3210
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186773896"
variation 3215
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377660053"
variation 3222
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371315253"
variation 3225
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:10451100"
variation 3226
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10451101"
variation 3249
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:191195638"
variation 3295
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:745829"
variation 3300
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:115824806"
variation 3302
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:111376207"
variation 3321
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:114452427"
variation 3326
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374057256"
variation 3369
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:190248447"
variation 3380
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:142288665"
variation 3394
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:193162748"
variation 3395
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:17223442"
variation 3416
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146229026"
variation 3423
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:115522604"
variation 3431
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:12446991"
variation 3433
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:116829884"
variation 3436
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:2077294"
variation 3441
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:2077293"
variation 3442
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:17223484"
variation 3453
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138634550"
variation 3462
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:375290907"
variation 3463
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:118124407"
variation 3464
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181400384"
variation 3475
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:184094351"
variation 3482
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:745828"
variation 3484
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:188384934"
variation 3492
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:75123725"
variation 3511..3513
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="agac"
/replace="caga"
/db_xref="dbSNP:3074250"
variation 3518
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="caga"
/db_xref="dbSNP:35534520"
variation 3541
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:369486130"
variation 3562
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:371462310"
variation 3576..3578
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gag"
/db_xref="dbSNP:368364143"
variation 3576
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:200762344"
variation 3590
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:11645658"
variation 3602
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142721966"
variation 3627
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:180748354"
variation 3637
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:187438076"
variation 3661
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:77128678"
variation 3686
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:137986488"
variation 3697
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:191806485"
variation 3700
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:149390717"
variation 3719
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:182395764"
variation 3728
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144795601"
variation 3729
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186942031"
variation 3749
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148569408"
variation 3766
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:143040860"
variation 3773..3774
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="g"
/db_xref="dbSNP:35503282"
variation 3780
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:78952726"
variation 3793
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:140020147"
variation 3802
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:190437215"
variation 3804
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:890895"
variation 3825
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:117343939"
variation 3844
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:182637485"
variation 3880
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:143600831"
variation 3921
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3803598"
variation 3935
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:139318371"
variation 3941
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:149921774"
variation 3956
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144992089"
variation 3981..3984
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="aagg"
/db_xref="dbSNP:139073845"
variation 3984..3987
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gaag"
/db_xref="dbSNP:369498159"
variation 3991
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:60991168"
variation 3994
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:189769746"
variation 3995
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:745161"
variation 4003
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376368123"
variation 4010
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:74912224"
variation 4011
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:11646569"
variation 4033
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142196871"
variation 4054
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:146148995"
variation 4055
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:118134388"
variation 4062
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:34082245"
variation 4081
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:890894"
variation 4089
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:111284148"
variation 4108
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:11646611"
variation 4129
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:141079929"
variation 4132
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143446071"
variation 4134
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:182067064"
variation 4145
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147999056"
variation 4155
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:890893"
variation 4172
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:115063113"
variation 4192
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:76440897"
variation 4195
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370561834"
variation 4207..4208
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:199566882"
variation 4216..4217
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="t"
/db_xref="dbSNP:374676848"
variation 4224
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:189066241"
variation 4235
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:374533934"
variation 4241
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:368953671"
variation 4247
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:141675314"
variation 4250
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374273825"
variation 4264
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10852351"
variation 4270
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3826099"
variation 4282
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150122382"
variation 4288
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:3826100"
variation 4294
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142999416"
variation 4300
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:28417794"
variation 4302
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:114317052"
variation 4306
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:149343231"
variation 4308
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372107842"
variation 4311
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:144686345"
variation 4337
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148516611"
variation 4349
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:142859735"
variation 4354
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:79809067"
variation 4355
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:115897036"
variation 4360
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:151075481"
variation 4370
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:193148810"
variation 4377
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:140493597"
variation 4396
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:185638841"
variation 4397
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:7500078"
variation 4417
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:147837528"
variation 4425
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:192060893"
variation 4446
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184242112"
variation 4456
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141460054"
variation 4470
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:188525258"
variation 4473
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:150385924"
variation 4481
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:144882460"
variation 4524
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3826101"
variation 4580
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:36021485"
variation 4588
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:149045999"
variation 4605
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143075871"
variation 4616
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:180902875"
variation 4630
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138597718"
variation 4643..4645
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="atg"
/db_xref="dbSNP:376723928"
variation 4647
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142907959"
variation 4657..4658
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="cg"
/replace="gg"
/db_xref="dbSNP:151150050"
variation 4658..4659
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="a"
/replace="ag"
/replace="g"
/replace="gg"
/db_xref="dbSNP:3842349"
variation 4658..4659
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ag"
/replace="gg"
/db_xref="dbSNP:72530769"
variation 4658
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:371931805"
variation 4659..4660
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ag"
/replace="gg"
/db_xref="dbSNP:67933888"
variation 4661
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:150033018"
variation 4663
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199839869"
variation 4675
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184547348"
variation 4677
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:75970447"
variation 4679
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:74875094"
variation 4687
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3826102"
variation 4688
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189422590"
variation 4699
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:56397350"
variation 4716
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:12927563"
variation 4723
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:138998254"
variation 4739
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373353831"
variation 4743
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141567333"
variation 4755
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150912062"
variation 4770
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:377508388"
variation 4776
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138145372"
variation 4793..4794
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ggg"
/db_xref="dbSNP:150264209"
variation 4794..4795
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gag"
/replace="ggg"
/db_xref="dbSNP:72530770"
variation 4795..4796
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gga"
/replace="ggg"
/db_xref="dbSNP:35339898"
variation 4796
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:28485829"
variation 4825
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:187286004"
variation 4839
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:149573066"
variation 4857
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:113199304"
variation 4875
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:115581496"
variation 4876
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:140819392"
variation 4894
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:144378107"
variation 4947
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:3826103"
variation 4950
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147401267"
variation 4957
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:190590673"
variation 4958
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:139695864"
variation 4959
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:142690853"
variation 4963
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181416690"
variation 4964
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:28605243"
variation 4965
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369119141"
variation 4979
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3803602"
variation 4987
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:185500939"
variation 5001
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:151021585"
variation 5023
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:189922080"
variation 5025..5027
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="cag"
/db_xref="dbSNP:148574478"
variation 5033
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:183261662"
variation 5037
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:187727380"
variation 5039
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:190959908"
variation 5061
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:183998970"
variation 5072..5073
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="aa"
/db_xref="dbSNP:202206141"
variation 5075
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:62028747"
variation 5090
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:140663791"
variation 5104
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:149667603"
variation 5110
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376105227"
variation 5113
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146687174"
variation 5152
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370123758"
variation 5164
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:140297867"
variation 5167
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:7198325"
variation 5181
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:372558683"
variation 5187
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:145381313"
variation 5193
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3803603"
variation 5207
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138943691"
variation 5208
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:187774662"
variation 5216
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372968012"
variation 5217
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:192201277"
variation 5223
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184364297"
STS 5226..5339
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="SHGC-61125"
/db_xref="UniSTS:9617"
variation 5228
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:187515232"
variation 5238
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:143813520"
variation 5246
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:7198503"
variation 5247
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148168698"
variation 5262
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:3803604"
variation 5281
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:191924957"
variation 5289..5291
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="tct"
/db_xref="dbSNP:200316654"
variation 5291
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:184824822"
variation 5296
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141814454"
variation 5297
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147250706"
variation 5342
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:139104092"
variation 5346
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:143087966"
variation 5355..5356
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ag"
/db_xref="dbSNP:374634837"
variation 5382
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:79162952"
variation 5389
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:75321034"
variation 5435
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147496154"
variation 5445
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:189284475"
variation 5454
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376197795"
variation 5467
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:78423456"
variation 5475
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:139143534"
variation 5485
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:114255545"
variation 5520
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:114977260"
variation 5533
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:149934302"
variation 5547..5548
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ag"
/db_xref="dbSNP:373613429"
variation 5563..5564
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ga"
/db_xref="dbSNP:71711881"
variation 5577
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:192623658"
variation 5587
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:371053231"
variation 5625
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144093655"
variation 5632
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:185618534"
variation 5648
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:372462302"
variation 5655
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685154"
variation 5656
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:76433792"
variation 5671
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3826104"
variation 5677
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371481334"
variation 5683
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375859589"
variation 5718
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:189166009"
variation 5738
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:202010384"
variation 5771
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143130623"
variation 5788
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146661411"
variation 5790
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:140248767"
variation 5810
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144039865"
variation 5815
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:146465887"
variation 5831
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:140529430"
variation 5853
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:181558975"
variation 5901
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:150456058"
variation 5902
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:114543851"
variation 5917
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138311312"
variation 5925
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:116469954"
variation 5926
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3803605"
variation 5951
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:149222146"
variation 5970
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186048559"
variation 5975
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371002229"
variation 5976
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:114219590"
variation 5982
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:17822411"
variation 5993
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:188899090"
variation 6027
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:139033688"
variation 6102
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376318225"
variation 6121
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:3803606"
variation 6158
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:58203085"
variation 6160
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:377181818"
variation 6166
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181402004"
variation 6182..6183
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="g"
/db_xref="dbSNP:11407600"
variation 6185
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:79377755"
variation 6194
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:186419640"
variation 6218
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:117922914"
variation 6220
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:9673974"
variation 6225
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147052454"
variation 6263
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:190858530"
variation 6270
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:370678985"
variation 6272
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:199815175"
variation 6281
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:182654806"
variation 6284..6285
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="tg"
/db_xref="dbSNP:372750353"
variation 6297
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3948441"
variation 6313
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:28470637"
variation 6330
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:148114457"
variation 6338
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:186453192"
variation 6341
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:73512066"
variation 6345
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:150566821"
variation 6369
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:191227558"
variation 6374
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:72775264"
variation 6378
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:76042295"
variation 6399
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3826105"
variation 6402
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:146286513"
variation 6407..6408
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="t"
/db_xref="dbSNP:71927283"
variation 6407
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:8061734"
variation 6421
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200723808"
variation 6435
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:143993911"
variation 6438
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369089568"
variation 6442
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:144921407"
variation 6444
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:371851177"
variation 6445
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373850437"
variation 6457
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:3803607"
variation 6472
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148643207"
variation 6476
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142904448"
variation 6479
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:3803608"
variation 6480..6481
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="cc"
/replace="gt"
/db_xref="dbSNP:377491840"
variation 6486
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3803609"
variation 6520..6521
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="a"
/db_xref="dbSNP:147727080"
variation 6520
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:183344441"
variation 6522..6523
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="a"
/db_xref="dbSNP:3840042"
variation 6535
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:13329697"
variation 6543
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3803610"
variation 6551
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:187630634"
variation 6560
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:151085158"
variation 6599
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:200170287"
variation 6600
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142586201"
variation 6625
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370722590"
variation 6630
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:146902486"
variation 6640
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:193066148"
variation 6642
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147960163"
variation 6654
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:115620406"
STS 6682..6815
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="RH66309"
/db_xref="UniSTS:19565"
variation 6684
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:183099969"
variation 6705
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:368813703"
variation 6707
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:112414053"
variation 6714
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:373587979"
STS 6722..6972
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="SHGC-60616"
/db_xref="UniSTS:12446"
STS 6728..6837
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="D16S2570E"
/db_xref="UniSTS:88139"
STS 6729..6892
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="RH25185"
/db_xref="UniSTS:84507"
variation 6757
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:79525599"
variation 6760
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:375094823"
variation 6771
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:141498213"
variation 6775
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147042065"
variation 6782
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371482828"
variation 6792
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375500698"
variation 6812
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:188129941"
variation 6869
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:192354933"
variation 6892
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:138190508"
variation 6909
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:34705637"
variation 6921
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143305107"
variation 6931
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:148245424"
variation 6934
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:11542102"
variation 6943
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:141789627"
variation 6954
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146260444"
variation 6974..6975
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ta"
/db_xref="dbSNP:201129580"
variation 6986
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184254310"
variation 7002
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:4780453"
variation 7055
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:9924027"
variation 7084
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:188141052"
variation 7086
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:192658619"
variation 7094
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10609"
variation 7116..7117
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="a"
/db_xref="dbSNP:34084585"
variation 7125
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:184636638"
variation 7129
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189035746"
variation 7140
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:181675488"
variation 7154
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:12477"
variation 7220
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186398163"
variation 7249
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:139414541"
variation 7250
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:78175785"
variation 7255
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:3803613"
variation 7278
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:142319322"
variation 7280
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189675689"
variation 7285
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:11542103"
variation 7303
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:375349417"
variation 7317
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:150513122"
variation 7322
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181273297"
variation 7342
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369149120"
variation 7343
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:139480078"
variation 7351
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:185484535"
variation 7352
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:11640862"
variation 7357
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:149692295"
variation 7383
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:377693516"
variation 7384
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:3803614"
variation 7410
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374064322"
variation 7411
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3169267"
variation 7427
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:3169266"
variation 7433
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:145535207"
variation 7434
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:140881705"
variation 7444
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:376621689"
variation 7464
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:370272174"
variation 7468
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:373704933"
variation 7507
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:28622434"
variation 7519
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189795476"
variation 7522
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:368561699"
variation 7523
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:183504990"
variation 7536
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:372281920"
variation 7544
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:186347281"
variation 7582
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:144829612"
variation 7586
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:147949386"
variation 7587
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374608454"
variation 7607
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:10500383"
variation 7633
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141875642"
variation 7635
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:376252607"
variation 7650
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:375762095"
variation 7663
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:151031035"
variation 7665
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:3169265"
variation 7709
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="c"
/db_xref="dbSNP:201835537"
variation 7719..7720
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="ggat"
/db_xref="dbSNP:367713038"
variation 7723..7725
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="aag"
/db_xref="dbSNP:146596498"
variation 7725..7727
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace=""
/replace="gaa"
/db_xref="dbSNP:370712901"
variation 7728
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:191653950"
variation 7737
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:140961090"
variation 7745
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:183498429"
variation 7763
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:372383994"
variation 7772
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:150216513"
variation 7780
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376099141"
variation 7787
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:114844137"
variation 7791
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138813745"
variation 7805
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:187989271"
variation 7807
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:9452"
variation 7808
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:140316578"
variation 7822
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:193002881"
variation 7830
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:145472350"
variation 7833
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:182494434"
variation 7862
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:186772773"
variation 7897
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:7619"
variation 7899
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:191184959"
STS 7908..8087
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="A005X12"
/db_xref="UniSTS:2299"
STS 7908..8087
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/standard_name="G20567"
/db_xref="UniSTS:2300"
variation 7920
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:184769020"
variation 7922
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138093059"
variation 7926
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1061008"
variation 7950
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:142647472"
variation 7963
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:7620"
variation 7965
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:144171185"
variation 7968
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:188908374"
variation 7972
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:192913461"
variation 7983
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:148191616"
variation 7991
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141156766"
variation 8004
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:377279144"
variation 8024
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369762033"
variation 8066
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:185480047"
variation 8103
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150733445"
variation 8108
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:139584133"
variation 8146
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:117110554"
variation 8152
/gene="SNX29"
/gene_synonym="A-388D4.1; RUNDC2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:117030210"
ORIGIN
ggcagccgcagaagcggcagcggcggcggcgcggcgcaggcaccggcccggggagaggcaccatgagcggatcacagaacaatgacaaaagacaatttctgctggagcgactgctggatgcagtgaaacagtgccagatccgctttggagggagaaaggagattgcctcggattccgacagcagggtcacctgtctgtgtgcccagtttgaagccgtcctgcagcatggcttgaagaggagtcgaggattggcactcacagcggcagcgatcaagcaggcagcgggctttgccagcaaaaccgaaacagagcccgtgttctggtactacgtgaaggaggtcctcaacaagcacgagctgcagcgcttctactccctgcgccacatcgcctcagacgtgggccggggtcgcgcctggctgcgctgtgccctcaacgaacactccctggagcgctacctgcacatgctcctggccgaccgctgcaggctgagcactttttatgaagactggtcttttgtgatggatgaagaaaggtccagtatgcttcctaccatggcagcaggtctgaactccatactctttgcgattaacatcgacaacaaggatttgaacgggcagagtaagtttgctcccaccgtttcagacctcttaaaggagtcaacgcagaacgtgacctccttgctgaaggagtccacgcaaggagtgagcagcctgttcagggagatcacagcctcctctgccgtctccatcctcatcaaacctgaacaggagaccgaccccttgcctgtcgtgtccaggaatgtcagtgctgatgccaaatgcaaaaaggagcggaagaagaaaaagaaagtgaccaacataatctcatttgatgatgaggaagatgagcagaactctggggacgtgtttaaaaagacacctggggcaggggagagctcagaggacaactccgaccgctcctctgtcaatatcatgtccgcctttgaaagccccttcgggcctaactccaatggaagtcagagcagcaactcatggaaaattgattccctgtctttgaacggggagtttgggtaccagaagcttgatgtgaaaagcatcgatgatgaagatgtggatgaaaacgaagatgacgtgtatggaaactcatcaggaaggaagcacaggggccactcggagtcgcccgagaagccactggaagggaacacctgcctctcccagatgcacagctgggctccgctgaaggtgctgcacaatgactccgacatcctcttccctgtcagtggcgtgggctcctacagcccagcagatgcccccctcggaagcctggagaacgggacaggaccagaggaccacgttctcccagatcctggacttcggtacagtgtggaagccagctctccaggccacggaagtcctctgagcagcctgttaccttctgcctcagtgccagagtccatgacaattagtgaactgcgccaggccactgtggccatgatgaacaggaaggatgagctggaggaggagaacagatcactgcgaaacctgctcgacggtgagatggagcactcagccgcgctccggcaagaggtggacaccttgaaaaggaaggtggctgaacaggaggagcggcagggcatgaaggtccaggcgctggccagagagaacgaggtgctcaaagtccaactgaagaaatatgtaggagctgtccagatgctgaaaagagaaggtcaaacagctgaagtgccaaatctttggagtgttgatggagaagttacagtagctgaacagaagccgggagaaattgctgaagaactcgcaagctcctacgaaagaaagctcatcgaggtggcagagatgcatggcgagctgattgagttcaacgagcgcctgcacagggccctggtagccaaggaagccctcgtgtcccagatgaggcaggagctcatcgatctccggggaccggtgcctggagatttgagtcaaacgtccgaagaccagagtttgtcggattttgaaatatcaaaccgggcgctgatcaacgtctggatcccctcagtgtttctccggggcaaagcagcaaatgcattccacgtgtatcaggtctacatccggataaaagacgatgaatggaatatttatcgccggtatacagagttcaggagtttgcaccacaagttacaaaacaagtaccctcaagtgagggcctacaacttcccacccaaaaaggccattggaaacaaggatgccaagtttgtggaggaacggagaaagcagctccagaattacctgcgcagcgtcatgaacaaagtcatccagatggtccccgagttcgctgccagccccaagaaggagaccctcatccagctgatgcccttcttcgtcgacatcaccccgcccggagagcctgtgaacagccggcccaaagcagcttcccgcttccccaaactgtcccggggtcagccccgggagacccgcaacgtggagccccagagcggtgacctctgacctcgacaaaaccgcagccacgggccctgtgcgtggcaccagctgcgtccaccccagccactgccgctggcccctcacctcagcgtgacaaccacgtccacctggtgatcctgagagcacacgattcccaacagttacacaacaccccgattaaactaatcagtcttcgagccgcatgataccgtgacccgagagaccaaggcagcacctcgctggagagactgggacacacagtccttctgcttctggggtctaccctgggctgcaagggctgttcctccacctttctgtagttcagggctggcaggagggtgggcaccaggtcaggctgggtgcgccatggttgagaggcaaaggtgatcccctatataggaaggttcatgcagagccagcctctccactctttcccacgtggggactagaatgactattagcctctccttttgctttttaaggttattacctggcctaacctagggatggctggctttgcgggggggggggggggggggggcatggttcctttcactgcattttccaccaacagtcattagacacctggcactgtcacagctcacttttccagagggatattcctgtggctttggcaaggagccattagtgatgtgcaacttgagttcagagaacttcccctacctcccccatggctggcttcaggaaggaccagtgccctccatagcctgaggccacctaggccctcgccaggcttggagtggggggactcagacatctggcccagccatcagcagcaacctagtaacccggcgtcatccagcgtgtccaaagtagcattggccctacagtcatgagagacttgggtcagggaaccactgcagaaggttccagggttttcaaaccaggctccatgactatgaagttggacccagtgtggacacttaacagatcatgtgtctctccactaaaaacattttccatcccgtctgcccccgacattgtccttgataacagaactctgcatcccctaagacagagtcctctgttcctcccatgtcaggtggctctcagagtacagggaccttggcaggtggagaggaggatggggaccagcagctgggcagcccccagggctcctcctccagtgagctcacatcagagcacctcacagagcaatagccgtcctcagatgctcagcaaagttgtggcagtttgcatttctagggtaaactaactaggaaggatgtcgtgaaatggactatgcaagagtaagtttgtgtgtttcgccttaatctgaggcagagacacagcagaacctgaggagaaaagcaggtggaaggtgacggttagatggtaagccatgggcttgtcctggaactgcttcaactcagtggcttaaaatgagaactgcccaggtgagcatggagcatctcctaggctcgaggacatctctggagaatcatctggaaggtttatactgtgccttcccctcgtagcaaaaaggaagattgttcatggcctttaaggaaggctgagatcactcacacacagcgcccccccaccccagagaaaccgagtcagcctacatgacttccaaggggacctggggccagataagccctgccccggtgagaccaaatgagctggagcatgtatggaggtgcggaccctgcagtcagtttgcgagtgtggaggacccgagacatcctgtaaaggcaacttggtctccctcccactcacctgccaacattgctgcaatacacatggtttatctgaaattccaaggccagagtgcacatcagctcacatgactggcaactctaaatagagagccctaatggactgaggcaggaaacgtctaaaagctcaatctgctgtatgtcatgaccccttaggttgggtttatgccacatcggtcattttgaagtaggtgtttgatgccagctcagagactgtctcaggagtgcctccctggcctgggtagctaccctggaggtcatctccctgttctctgttggataaaggaacctcccccatctgtgacattcccttgggcccaggcttatgacctgcaccttttctgacacctgcccccaaagcacaggatgtgaattggtctctctccagataccccacgaggaagcaccttggacattctgcacatgataataatgcaacagtcccccattgctgagagatactaacccgtgagaaacaagtatgctctcagctggtattgaactggtgggagaaactgcctcctacttttataatactgaattattcacaaaaaacctggtctgctctccaaaatgagagcatgttcctgggagccacatggggaccatccccagctgcctgctcctggtacctcccccatgatcatgcacagaccgtagagtcgagtcatctcgcagatccagaccatctcctctcattctcactctaaaaatgctggtggcccgcacatgacagcaactccccgaagccttccctttggaatcccatagaatgttctgcaatgattgggtccatcttgctgctcagaagaatcccgtcctgctctctagtgtggtgggatgaacttcaggcaacaaacaactggcagggttcccagttcctggagttatggagcagaaacacccaggcctagcagaattgtggctgaaacctggtgcccaaattccacaccctggaaatgtgtcaactgcctgtcagcctggattcaattctgagggctaagccacgaccttatccatgagtggcgaagacacccctgaggaaaggattgcttgcacctcacatctgtcttcttctaagattactcggagattttcaaacaacatctgagaacagaagccccctcccctactcagagaggaacgagggtggcccacctctcaagggccttggattcctgggaccaccctttgctgggaggaagaatccacaccgaatccttctgtcttcatggcctgctgtgctgaaacagaacagcaggttccatctttcacatctttttttctcccccagatgaaagacgactcaggaacggtagggctgggcagaggtgtctctccttgagagacaacaaaagcttctaagggagggagcttaaaggctgctagaaacctagcccaaccatccactcctgatctgagacagaaccttctccgccactcttcctgcaatcagtgtgaaattccagcttctttgattcccacttagcagtatgctccaatcacgttgctggcaaggcattttagagtttggagctgaggttcaaagccccctgcatttctctactggcaggccctggtgaaggaagacactttcagggaagaggctcttacagtctatggtggtagccatcttcacatccagtcaccagttgcatctagggagctgctggctataaaagggatcatccagtggagttgtaaacaagggaaccatcttgcaagatctaggaagaggaaggggagggatgtggactgggtctgatcacagcccttggccctgcttcatactttggagcttattaagatcaattttgataaccatgtaatttcttagaaccatggcaggtagtattgtgctttaaaaaccagaggctcctgaaagtcgtttacaccaggtggattgataccatggctgtagctgatgcaactaacaagtactggggccagtgatcacaatccaggttggaaacaggagtgaagcccaccagcctgcctggttgatggacagcaggctctgccttctggaggcggcttatatcccaacagcctgaggcagggctctgtggcccaggccggcagtggctgcctctcttggttctgcatggtacattttgccaaccctgaggaccagttcttggggttccaggcctcggccttcctgctccacgtgctcaagcccccacagggggctgcgacaccatctggctcctcacagggaggtccagccatgttctctgggctcccagtgagccccctcccctccggctacccccagaatccatccttcattcctccaccaagctcctgtgtgagctgcagcacccacacgggggaagccctgcactccagcagcatcttccagccttggcacagaactgatggcaaaggaagggctgggttttcagcttctgggacccgaggaagaccccacctcactcctccttccccagtacatcagactggttaggaggcatcccagaaggggcagcctcatgcccaggtttcagccctaaaggtaatgattgtcttgactctgccttggcatttcgctcggaatcacggcagacttggagtgtttcttcaaggcaggcatctgcttatgagcaaggtcaaagatttttcaaaatattgtgcattaattcattaaagctactgttaaatatttgctgtttttagattggcgtccgtgctaattctgcagttgtagcactgtatattttatctcatttctgtgccaagaaagttcatctttatgtttttctaatacacaatcttgatcttgtttccaaaataaagcttcagctccttggtcaatagaagtaagggtgtagccatccagggtctcccggctctaggcagaccggatcccgcagttcatcccatggttgttgaaatgtacctcgatcagtcatctctggtattcctcactctagccatgagccattgccatcttatgggcccgatttgggtactctgaattatgtcatggagtagacagttacttctaaatcccagcaaccaagttgcgtatccttccttatagctagtttctatagagaagtgaaaaagaaatctggcttccttaataagatagttgagcctatgacattaaggagcagcgctgctggcggaagattctagattcactggtggtttaagaggcccagggatttagttcttactggtgcgtaagtgttttcccatcctaaccggaaaaccactcacccaggcttcccccacttcccctcaaattttctcagctctgccgctggtctccatgaacggcaaggggaaccaccactcattcactgtcagtgtaggtaagacagaggatgcccttgcaaaaattgggactgaggacagtagcacacggaatggtggatcgtacatttgcacccagagctactaaacgctcagtgaccccagagaccattaatttcccggagtgaaggggatgggggtagagctaattggaatttttattatccaggactcatcctaagaagaatgttggcctctcttcatccctggcttagccgtcaggtagaacgcttactcacctgacaccgacttcttagagaagcgagtcttttttgaatggaggagcgatggtaaccccactagggggcgcccatgatcggctcccagtgcacccccttaagggtaagcaggccacatatctagagtctgatagtctgtgtgtacataaggtctagaagtctgtggaaacgccctgaaacctgtagtattatcttaactaccctcttatgttaaggtttacataataggatttttaaacaaatgtgtttaattttttaagatctcttgtattaaaattttcttttggaataagctgtggaaattttgttacaacctggttgagatcaacctctttacaatgacacaaattgtgacattttataaattagatacttcagtggaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:92017 -> Molecular function: GO:0035091 [phosphatidylinositol binding] evidence: IEA
GeneID:92017 -> Biological process: GO:0007154 [cell communication] evidence: IEA
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@meso_cacase at
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