ClinVar Miner

List of variants in gene SLC2A10 reported as likely benign for not specified

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Gene type:
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Total variants: 51
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HGVS dbSNP
NM_030777.4(SLC2A10):c.*8G>A rs375282462
NM_030777.4(SLC2A10):c.-15C>T rs377142129
NM_030777.4(SLC2A10):c.-26dup rs1335581409
NM_030777.4(SLC2A10):c.1110T>C (p.Thr370=) rs760859018
NM_030777.4(SLC2A10):c.1208G>A (p.Arg403Gln) rs199912561
NM_030777.4(SLC2A10):c.1212G>T (p.Gly404=) rs139155480
NM_030777.4(SLC2A10):c.1225C>T (p.Arg409Cys) rs562212724
NM_030777.4(SLC2A10):c.1269C>T (p.Phe423=) rs1057524067
NM_030777.4(SLC2A10):c.1289-6C>T rs199967429
NM_030777.4(SLC2A10):c.1299T>C (p.Leu433=) rs879632885
NM_030777.4(SLC2A10):c.1305C>T (p.Leu435=) rs201159437
NM_030777.4(SLC2A10):c.1371G>A (p.Ala457=) rs558894862
NM_030777.4(SLC2A10):c.1401C>T (p.Leu467=) rs774586341
NM_030777.4(SLC2A10):c.1412-13C>T rs371888996
NM_030777.4(SLC2A10):c.1412-3C>T rs374857656
NM_030777.4(SLC2A10):c.1446C>T (p.Tyr482=) rs150398871
NM_030777.4(SLC2A10):c.1461C>T (p.Val487=) rs1555888585
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.1547+19G>A rs546525339
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn) rs573480396
NM_030777.4(SLC2A10):c.1605C>T (p.Ile535=) rs148470005
NM_030777.4(SLC2A10):c.1617G>A (p.Ala539=) rs114974138
NM_030777.4(SLC2A10):c.180C>T (p.Leu60=) rs371988251
NM_030777.4(SLC2A10):c.237C>A (p.Leu79=) rs201323237
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=) rs150800734
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly) rs144095826
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.369G>C (p.Val123=) rs1555887891
NM_030777.4(SLC2A10):c.4+9C>G rs1057521373
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.54T>C (p.Gly18=) rs772186491
NM_030777.4(SLC2A10):c.587A>T (p.Lys196Met) rs145446653
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.630C>T (p.Gly210=) rs142431229
NM_030777.4(SLC2A10):c.633G>A (p.Pro211=) rs770919957
NM_030777.4(SLC2A10):c.635G>C (p.Gly212Ala) rs863223730
NM_030777.4(SLC2A10):c.644G>A (p.Arg215Gln) rs774497964
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His) rs34295241
NM_030777.4(SLC2A10):c.720C>A (p.Leu240=) rs374985824
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=) rs142106322
NM_030777.4(SLC2A10):c.792T>C (p.His264=) rs377031320
NM_030777.4(SLC2A10):c.794G>C (p.Gly265Ala) rs863223731
NM_030777.4(SLC2A10):c.810G>C (p.Val270=) rs774452914
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=) rs148058006
NM_030777.4(SLC2A10):c.873G>A (p.Val291=) rs755197578
NM_030777.4(SLC2A10):c.918C>T (p.Leu306=)
NM_030777.4(SLC2A10):c.948C>T (p.Leu316=) rs755109002

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