ClinVar Miner

List of variants in gene SLC2A10 studied for not provided

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Gene type:
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Total variants: 107
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HGVS dbSNP
GRCh37/hg19 20q13.12(chr20:45350682-45499090)x3
NC_000020.11:g.46709416C>A rs73115554
NC_000020.11:g.46709464C>T rs137938281
NM_030777.4(SLC2A10):c.1010G>C (p.Gly337Ala) rs150745395
NM_030777.4(SLC2A10):c.1014G>C (p.Gln338His) rs35833600
NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=) rs1301992983
NM_030777.4(SLC2A10):c.1057C>G (p.Leu353Val) rs200196034
NM_030777.4(SLC2A10):c.1096C>T (p.Pro366Ser) rs774664650
NM_030777.4(SLC2A10):c.110_121del (p.Gln37_Gly41delinsArg)
NM_030777.4(SLC2A10):c.1175G>A (p.Ser392Asn) rs863223733
NM_030777.4(SLC2A10):c.1191G>A (p.Gly397=) rs750216918
NM_030777.4(SLC2A10):c.1206T>A (p.Ala402=)
NM_030777.4(SLC2A10):c.1219C>T (p.Leu407=) rs1194888660
NM_030777.4(SLC2A10):c.1233C>T (p.Thr411=) rs778452693
NM_030777.4(SLC2A10):c.1265C>T (p.Ala422Val) rs1600668873
NM_030777.4(SLC2A10):c.1269C>T (p.Phe423=) rs1057524067
NM_030777.4(SLC2A10):c.1276G>T (p.Gly426Trp) rs121908172
NM_030777.4(SLC2A10):c.1278_1287delinsCC (p.Phe427fs) rs1064796832
NM_030777.4(SLC2A10):c.1299T>C (p.Leu433=) rs879632885
NM_030777.4(SLC2A10):c.129C>G (p.Ser43Arg) rs863223734
NM_030777.4(SLC2A10):c.1305C>T (p.Leu435=) rs201159437
NM_030777.4(SLC2A10):c.1309G>A (p.Glu437Lys) rs763220502
NM_030777.4(SLC2A10):c.1324G>C (p.Glu442Gln) rs143265363
NM_030777.4(SLC2A10):c.1330C>T (p.Arg444Ter) rs370547023
NM_030777.4(SLC2A10):c.1334del (p.Gly445fs) rs587776600
NM_030777.4(SLC2A10):c.1344C>T (p.Phe448=) rs553831434
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val) rs201393026
NM_030777.4(SLC2A10):c.1371G>A (p.Ala457=) rs558894862
NM_030777.4(SLC2A10):c.1377C>T (p.Asn459=) rs756207829
NM_030777.4(SLC2A10):c.1402G>A (p.Asp468Asn) rs768345011
NM_030777.4(SLC2A10):c.1411+176G>C rs775643873
NM_030777.4(SLC2A10):c.1411+181del rs201022621
NM_030777.4(SLC2A10):c.1411+2T>A rs761721442
NM_030777.4(SLC2A10):c.1412-114A>G rs1122067
NM_030777.4(SLC2A10):c.1415C>T (p.Thr472Ile) rs563376340
NM_030777.4(SLC2A10):c.1423T>G (p.Leu475Val) rs754355572
NM_030777.4(SLC2A10):c.1455C>T (p.Thr485=) rs1285063741
NM_030777.4(SLC2A10):c.1456G>A (p.Ala486Thr) rs759205774
NM_030777.4(SLC2A10):c.145T>A (p.Phe49Ile) rs863223729
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=) rs142639587
NM_030777.4(SLC2A10):c.1481A>G (p.Tyr494Cys) rs374854180
NM_030777.4(SLC2A10):c.1497A>G (p.Glu499=) rs780076629
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=) rs117587497
NM_030777.4(SLC2A10):c.1547+18del rs771439306
NM_030777.4(SLC2A10):c.1547+223G>T rs3091961
NM_030777.4(SLC2A10):c.1547+96C>T rs2425907
NM_030777.4(SLC2A10):c.1548-61C>G rs113249258
NM_030777.4(SLC2A10):c.1548G>T (p.Arg516=) rs116344406
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn) rs573480396
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys) rs370141550
NM_030777.4(SLC2A10):c.1600C>T (p.Arg534Cys) rs142577271
NM_030777.4(SLC2A10):c.1601G>A (p.Arg534His) rs746480018
NM_030777.4(SLC2A10):c.1616C>T (p.Ala539Val) rs140312420
NM_030777.4(SLC2A10):c.163C>T (p.Leu55Phe) rs745611450
NM_030777.4(SLC2A10):c.195T>A (p.Gly65=) rs1002286842
NM_030777.4(SLC2A10):c.212G>T (p.Cys71Phe) rs377305511
NM_030777.4(SLC2A10):c.237C>A (p.Leu79=) rs201323237
NM_030777.4(SLC2A10):c.238G>A (p.Gly80Arg) rs369865870
NM_030777.4(SLC2A10):c.243C>G (p.Ser81Arg) rs80358230
NM_030777.4(SLC2A10):c.254T>C (p.Leu85Pro)
NM_030777.4(SLC2A10):c.264C>G (p.Gly88=) rs768512276
NM_030777.4(SLC2A10):c.267C>T (p.Ser89=) rs747559824
NM_030777.4(SLC2A10):c.297C>T (p.Ala99=) rs1390850910
NM_030777.4(SLC2A10):c.306C>T (p.Val102=) rs530216827
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys) rs767864243
NM_030777.4(SLC2A10):c.314G>A (p.Arg105His) rs753280877
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr) rs6094438
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile) rs373375540
NM_030777.4(SLC2A10):c.363C>T (p.Ile121=) rs1164117855
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=) rs34990188
NM_030777.4(SLC2A10):c.371C>T (p.Ser124Leu) rs774076515
NM_030777.4(SLC2A10):c.383G>A (p.Gly128Glu) rs1226198239
NM_030777.4(SLC2A10):c.416A>G (p.Tyr139Cys) rs139858464
NM_030777.4(SLC2A10):c.430A>T (p.Thr144Ser) rs748746893
NM_030777.4(SLC2A10):c.443T>C (p.Leu148Pro) rs863223732
NM_030777.4(SLC2A10):c.455C>T (p.Ala152Val) rs775987124
NM_030777.4(SLC2A10):c.475G>T (p.Gly159Cys) rs761947206
NM_030777.4(SLC2A10):c.484T>C (p.Trp162Arg) rs755925085
NM_030777.4(SLC2A10):c.484del (p.Trp162fs)
NM_030777.4(SLC2A10):c.5-116A>G rs183563269
NM_030777.4(SLC2A10):c.5-121dup rs879560987
NM_030777.4(SLC2A10):c.5-9_5-7del rs1600666288
NM_030777.4(SLC2A10):c.504C>A (p.Phe168Leu) rs540023880
NM_030777.4(SLC2A10):c.505G>A (p.Gly169Ser) rs35151194
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile) rs143301610
NM_030777.4(SLC2A10):c.519A>G (p.Ala173=) rs747333286
NM_030777.4(SLC2A10):c.57C>T (p.Gly19=) rs1600666379
NM_030777.4(SLC2A10):c.633G>A (p.Pro211=) rs770919957
NM_030777.4(SLC2A10):c.663C>A (p.Leu221=) rs768433086
NM_030777.4(SLC2A10):c.666C>T (p.Phe222=) rs776448517
NM_030777.4(SLC2A10):c.673C>T (p.Arg225Cys) rs199659394
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His) rs34295241
NM_030777.4(SLC2A10):c.691C>T (p.Arg231Trp) rs146579504
NM_030777.4(SLC2A10):c.712C>G (p.Leu238Val) rs761633200
NM_030777.4(SLC2A10):c.731_734del (p.Leu244fs) rs864309481
NM_030777.4(SLC2A10):c.746A>G (p.Asn249Ser) rs531533787
NM_030777.4(SLC2A10):c.797G>T (p.Gly266Val) rs369484751
NM_030777.4(SLC2A10):c.848C>A (p.Ala283Asp) rs145994112
NM_030777.4(SLC2A10):c.859G>A (p.Ala287Thr) rs780058786
NM_030777.4(SLC2A10):c.876C>A (p.Asp292Glu) rs777604168
NM_030777.4(SLC2A10):c.878G>A (p.Arg293His) rs770882223
NM_030777.4(SLC2A10):c.915C>T (p.Ala305=) rs199975775
NM_030777.4(SLC2A10):c.920T>A (p.Met307Lys) rs768142427
NM_030777.4(SLC2A10):c.929C>T (p.Ser310Phe) rs763521707
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.995T>C (p.Val332Ala) rs570363463
NM_030777.4(SLC2A10):c.9C>T (p.His3=) rs1423610543

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