ClinVar Miner

List of variants in gene SLC2A10 reported as uncertain significance by Ambry Genetics

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Total variants: 24
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HGVS dbSNP
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.119T>C (p.Phe40Ser) rs372166877
NM_030777.4(SLC2A10):c.1274T>C (p.Phe425Ser) rs546176728
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.1457C>A (p.Ala486Asp) rs775211875
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.1616C>T (p.Ala539Val) rs140312420
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.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.455C>T (p.Ala152Val) rs775987124
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.680A>G (p.Asn227Ser) rs959288629
NM_030777.4(SLC2A10):c.781G>A (p.Val261Ile) rs372561968
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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