ClinVar Miner

List of variants in gene SLC2A10 reported as likely benign by Invitae

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=) rs370173604
NM_030777.4(SLC2A10):c.1010G>C (p.Gly337Ala) rs150745395
NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=) rs1301992983
NM_030777.4(SLC2A10):c.1079A>G (p.Asn360Ser)
NM_030777.4(SLC2A10):c.1185C>T (p.Leu395=)
NM_030777.4(SLC2A10):c.1187C>T (p.Pro396Leu) rs755654519
NM_030777.4(SLC2A10):c.1203C>T (p.Pro401=) rs368021257
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.1234G>A (p.Ala412Thr) rs746203433
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.1344C>T (p.Phe448=) rs553831434
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val) rs201393026
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.1401C>T (p.Leu467=) rs774586341
NM_030777.4(SLC2A10):c.1446C>T (p.Tyr482=) rs150398871
NM_030777.4(SLC2A10):c.1455C>T (p.Thr485=) rs1285063741
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=) rs142639587
NM_030777.4(SLC2A10):c.1497A>G (p.Glu499=) rs780076629
NM_030777.4(SLC2A10):c.1536C>T (p.Phe512=) rs745307904
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.1566C>T (p.Gly522=)
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys) rs370141550
NM_030777.4(SLC2A10):c.1593G>A (p.Pro531=) rs148424607
NM_030777.4(SLC2A10):c.1605C>T (p.Ile535=) rs148470005
NM_030777.4(SLC2A10):c.180C>T (p.Leu60=) rs371988251
NM_030777.4(SLC2A10):c.189G>C (p.Leu63=) rs890578209
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.315C>T (p.Arg105=) rs150800734
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr) rs6094438
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.363C>T (p.Ile121=) rs1164117855
NM_030777.4(SLC2A10):c.4+10G>A
NM_030777.4(SLC2A10):c.432C>T (p.Thr144=) rs371344477
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.581C>T (p.Thr194Ile) rs763889166
NM_030777.4(SLC2A10):c.599C>G (p.Pro200Arg) rs75218052
NM_030777.4(SLC2A10):c.621C>G (p.Pro207=)
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.633G>A (p.Pro211=) rs770919957
NM_030777.4(SLC2A10):c.645G>C (p.Arg215=)
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.674G>A (p.Arg225His) rs34295241
NM_030777.4(SLC2A10):c.681C>T (p.Asn227=)
NM_030777.4(SLC2A10):c.696C>G (p.Thr232=) rs138679634
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=) rs142106322
NM_030777.4(SLC2A10):c.780C>T (p.Ser260=) rs181500247
NM_030777.4(SLC2A10):c.792T>C (p.His264=) rs377031320
NM_030777.4(SLC2A10):c.810G>C (p.Val270=) rs774452914
NM_030777.4(SLC2A10):c.831C>A (p.Gly277=)
NM_030777.4(SLC2A10):c.831C>T (p.Gly277=)
NM_030777.4(SLC2A10):c.858C>T (p.Thr286=) rs758420381
NM_030777.4(SLC2A10):c.876C>A (p.Asp292Glu) rs777604168
NM_030777.4(SLC2A10):c.915C>T (p.Ala305=) rs199975775
NM_030777.4(SLC2A10):c.924C>T (p.Ala308=) rs377173165
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.948C>T (p.Leu316=) rs755109002
NM_030777.4(SLC2A10):c.960C>T (p.Ala320=)
NM_030777.4(SLC2A10):c.961G>A (p.Val321Met) rs372596900
NM_030777.4(SLC2A10):c.9C>T (p.His3=) rs1423610543

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