ClinVar Miner

List of variants in gene SLC2A10 studied for Cardiovascular phenotype

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Total variants: 55
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HGVS dbSNP
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=) rs370173604
NM_030777.4(SLC2A10):c.1018G>A (p.Gly340Ser) rs1333501401
NM_030777.4(SLC2A10):c.1087C>G (p.Gln363Glu) rs886038934
NM_030777.4(SLC2A10):c.1154C>G (p.Ala385Gly) rs79849424
NM_030777.4(SLC2A10):c.119T>C (p.Phe40Ser) rs372166877
NM_030777.4(SLC2A10):c.1212G>T (p.Gly404=) rs139155480
NM_030777.4(SLC2A10):c.1233C>T (p.Thr411=) rs778452693
NM_030777.4(SLC2A10):c.1274T>C (p.Phe425Ser) rs546176728
NM_030777.4(SLC2A10):c.1334del (p.Gly445fs) rs587776600
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val) rs201393026
NM_030777.4(SLC2A10):c.1412-3C>T rs374857656
NM_030777.4(SLC2A10):c.1415C>T (p.Thr472Ile) rs563376340
NM_030777.4(SLC2A10):c.144G>A (p.Glu48=) rs375145963
NM_030777.4(SLC2A10):c.1455C>T (p.Thr485=) rs1285063741
NM_030777.4(SLC2A10):c.1457C>A (p.Ala486Asp) rs775211875
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=) rs142639587
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=) rs117587497
NM_030777.4(SLC2A10):c.1541A>G (p.Lys514Arg) rs41283344
NM_030777.4(SLC2A10):c.1548G>T (p.Arg516=) rs116344406
NM_030777.4(SLC2A10):c.1552A>G (p.Thr518Ala) rs6018008
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.1609A>G (p.Ile537Val) rs7348121
NM_030777.4(SLC2A10):c.1616C>T (p.Ala539Val) rs140312420
NM_030777.4(SLC2A10):c.1617G>A (p.Ala539=) rs114974138
NM_030777.4(SLC2A10):c.237C>T (p.Leu79=) rs201323237
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys) rs767864243
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=) rs150800734
NM_030777.4(SLC2A10):c.316G>T (p.Ala106Ser) rs6094438
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly) rs144095826
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile) rs373375540
NM_030777.4(SLC2A10):c.330C>T (p.Phe110=) rs199848479
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=) rs34990188
NM_030777.4(SLC2A10):c.367G>A (p.Val123Met) rs770619266
NM_030777.4(SLC2A10):c.388C>T (p.Arg130Trp) rs201150247
NM_030777.4(SLC2A10):c.394C>T (p.Arg132Trp) rs121908173
NM_030777.4(SLC2A10):c.432C>T (p.Thr144=) rs371344477
NM_030777.4(SLC2A10):c.455C>T (p.Ala152Val) rs775987124
NM_030777.4(SLC2A10):c.504C>T (p.Phe168=) rs540023880
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile) rs143301610
NM_030777.4(SLC2A10):c.581C>T (p.Thr194Ile) rs763889166
NM_030777.4(SLC2A10):c.610G>A (p.Gly204Ser) rs755339268
NM_030777.4(SLC2A10):c.616G>A (p.Ala206Thr) rs2235491
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His) rs34295241
NM_030777.4(SLC2A10):c.680A>G (p.Asn227Ser) rs959288629
NM_030777.4(SLC2A10):c.685C>T (p.Arg229Ter) rs756457861
NM_030777.4(SLC2A10):c.692G>A (p.Arg231Gln) rs771028960
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=) rs142106322
NM_030777.4(SLC2A10):c.781G>A (p.Val261Ile) rs372561968
NM_030777.4(SLC2A10):c.792T>C (p.His264=) rs377031320
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=) rs148058006
NM_030777.4(SLC2A10):c.848C>A (p.Ala283Asp) rs145994112
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.949G>C (p.Val317Leu) rs781230863

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