ClinVar Miner

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

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Gene type:
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Total variants: 39
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HGVS dbSNP
NC_000020.11:g.46709416C>A rs73115554
NC_000020.11:g.46709464C>T rs137938281
NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=) rs1301992983
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.1269C>T (p.Phe423=) rs1057524067
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.1344C>T (p.Phe448=) rs553831434
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.1455C>T (p.Thr485=) rs1285063741
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.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.195T>A (p.Gly65=) rs1002286842
NM_030777.4(SLC2A10):c.237C>A (p.Leu79=) rs201323237
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.363C>T (p.Ile121=) rs1164117855
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=) rs34990188
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.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.915C>T (p.Ala305=) rs199975775
NM_030777.4(SLC2A10):c.9C>T (p.His3=) rs1423610543

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