ClinVar Miner

List of variants in gene SLC2A10 reported as uncertain significance by Invitae

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Gene type:
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Total variants: 88
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HGVS dbSNP
NC_000020.10:g.(?_45362375)_(45362493_?)del
NM_030777.4(SLC2A10):c.1002T>A (p.Asn334Lys)
NM_030777.4(SLC2A10):c.1009G>A (p.Gly337Arg) rs369238826
NM_030777.4(SLC2A10):c.104C>T (p.Pro35Leu)
NM_030777.4(SLC2A10):c.1057C>G (p.Leu353Val) rs200196034
NM_030777.4(SLC2A10):c.1087C>G (p.Gln363Glu) rs886038934
NM_030777.4(SLC2A10):c.1096C>T (p.Pro366Ser) rs774664650
NM_030777.4(SLC2A10):c.1154C>T (p.Ala385Val)
NM_030777.4(SLC2A10):c.115G>A (p.Asp39Asn) rs367623970
NM_030777.4(SLC2A10):c.1183C>T (p.Leu395Phe)
NM_030777.4(SLC2A10):c.119T>C (p.Phe40Ser) rs372166877
NM_030777.4(SLC2A10):c.1204G>A (p.Ala402Thr) rs147710229
NM_030777.4(SLC2A10):c.1208G>A (p.Arg403Gln) rs199912561
NM_030777.4(SLC2A10):c.1216G>A (p.Ala406Thr)
NM_030777.4(SLC2A10):c.1225C>T (p.Arg409Cys) rs562212724
NM_030777.4(SLC2A10):c.1274T>C (p.Phe425Ser) rs546176728
NM_030777.4(SLC2A10):c.1324G>C (p.Glu442Gln) rs143265363
NM_030777.4(SLC2A10):c.1351T>G (p.Cys451Gly) rs199599532
NM_030777.4(SLC2A10):c.1375A>C (p.Asn459His)
NM_030777.4(SLC2A10):c.1387A>C (p.Ser463Arg) rs771091234
NM_030777.4(SLC2A10):c.1402G>A (p.Asp468Asn) rs768345011
NM_030777.4(SLC2A10):c.1412-3C>T rs374857656
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.1426T>C (p.Ser476Pro)
NM_030777.4(SLC2A10):c.1443C>G (p.Leu481=)
NM_030777.4(SLC2A10):c.1465G>C (p.Gly489Arg)
NM_030777.4(SLC2A10):c.147C>G (p.Phe49Leu) rs1600666532
NM_030777.4(SLC2A10):c.1481A>G (p.Tyr494Cys) rs374854180
NM_030777.4(SLC2A10):c.1539G>C (p.Gln513His) rs1334989775
NM_030777.4(SLC2A10):c.1547G>A (p.Arg516Gln) rs760437795
NM_030777.4(SLC2A10):c.1547G>C (p.Arg516Pro) rs760437795
NM_030777.4(SLC2A10):c.1573del (p.Gln525fs)
NM_030777.4(SLC2A10):c.1586G>A (p.Gly529Asp) rs750292263
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.1606G>A (p.Glu536Lys) rs1238866581
NM_030777.4(SLC2A10):c.1611C>G (p.Ile537Met) rs1060502314
NM_030777.4(SLC2A10):c.170G>T (p.Gly57Val)
NM_030777.4(SLC2A10):c.193G>T (p.Gly65Cys)
NM_030777.4(SLC2A10):c.206T>C (p.Ile69Thr)
NM_030777.4(SLC2A10):c.209A>G (p.Asp70Gly)
NM_030777.4(SLC2A10):c.218G>A (p.Gly73Asp)
NM_030777.4(SLC2A10):c.252G>A (p.Val84=) rs878855129
NM_030777.4(SLC2A10):c.300G>C (p.Trp100Cys) rs886056725
NM_030777.4(SLC2A10):c.311G>A (p.Gly104Asp) rs1060502311
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys) rs767864243
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile) rs373375540
NM_030777.4(SLC2A10):c.367G>A (p.Val123Met) rs770619266
NM_030777.4(SLC2A10):c.368T>C (p.Val123Ala)
NM_030777.4(SLC2A10):c.388C>T (p.Arg130Trp) rs201150247
NM_030777.4(SLC2A10):c.395G>T (p.Arg132Leu) rs376346077
NM_030777.4(SLC2A10):c.397G>A (p.Gly133Arg) rs1555887907
NM_030777.4(SLC2A10):c.421G>A (p.Ala141Thr) rs756110797
NM_030777.4(SLC2A10):c.433G>A (p.Val145Met) rs772308135
NM_030777.4(SLC2A10):c.455C>T (p.Ala152Val) rs775987124
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.517G>A (p.Ala173Thr) rs1060502312
NM_030777.4(SLC2A10):c.530T>C (p.Leu177Pro) rs777214287
NM_030777.4(SLC2A10):c.533A>G (p.Gln178Arg)
NM_030777.4(SLC2A10):c.560C>T (p.Ala187Val)
NM_030777.4(SLC2A10):c.562G>C (p.Gly188Arg)
NM_030777.4(SLC2A10):c.577G>A (p.Ala193Thr) rs780965802
NM_030777.4(SLC2A10):c.5G>C (p.Gly2Ala) rs1555887782
NM_030777.4(SLC2A10):c.601C>T (p.Leu201Phe) rs199861432
NM_030777.4(SLC2A10):c.611G>A (p.Gly204Asp) rs1555887956
NM_030777.4(SLC2A10):c.646T>A (p.Tyr216Asn)
NM_030777.4(SLC2A10):c.65T>G (p.Phe22Cys) rs1060502313
NM_030777.4(SLC2A10):c.671C>G (p.Ala224Gly) rs371261694
NM_030777.4(SLC2A10):c.691C>T (p.Arg231Trp) rs146579504
NM_030777.4(SLC2A10):c.697A>C (p.Thr233Pro) rs190252962
NM_030777.4(SLC2A10):c.736G>A (p.Gly246Arg) rs1568985955
NM_030777.4(SLC2A10):c.781G>A (p.Val261Ile) rs372561968
NM_030777.4(SLC2A10):c.797G>A (p.Gly266Glu) rs369484751
NM_030777.4(SLC2A10):c.797G>T (p.Gly266Val) rs369484751
NM_030777.4(SLC2A10):c.808G>A (p.Val270Met)
NM_030777.4(SLC2A10):c.826C>A (p.Leu276Ile)
NM_030777.4(SLC2A10):c.848C>A (p.Ala283Asp) rs145994112
NM_030777.4(SLC2A10):c.873G>A (p.Val291=) rs755197578
NM_030777.4(SLC2A10):c.877C>T (p.Arg293Cys)
NM_030777.4(SLC2A10):c.878G>A (p.Arg293His) rs770882223
NM_030777.4(SLC2A10):c.886C>T (p.Arg296Cys)
NM_030777.4(SLC2A10):c.887G>A (p.Arg296His) rs558025597
NM_030777.4(SLC2A10):c.8A>C (p.His3Pro) rs1254965156
NM_030777.4(SLC2A10):c.920T>A (p.Met307Lys) rs768142427
NM_030777.4(SLC2A10):c.949G>A (p.Val317Ile)
NM_030777.4(SLC2A10):c.995T>C (p.Val332Ala) rs570363463

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