ClinVar Miner

List of variants in gene SPTAN1 reported as uncertain significance for not specified

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Total variants: 26
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HGVS dbSNP
NM_001130438.3(SPTAN1):c.1689G>T (p.Met563Ile) rs373973880
NM_001130438.3(SPTAN1):c.237+4C>T rs371350283
NM_001130438.3(SPTAN1):c.2599G>A (p.Glu867Lys) rs1339046005
NM_001130438.3(SPTAN1):c.2645G>A (p.Arg882His) rs1486021166
NM_001130438.3(SPTAN1):c.3042T>G (p.Gly1014=) rs150870424
NM_001130438.3(SPTAN1):c.3050C>T (p.Pro1017Leu) rs370748662
NM_001130438.3(SPTAN1):c.3079G>A (p.Ala1027Thr) rs779759134
NM_001130438.3(SPTAN1):c.3156-10C>T rs745910160
NM_001130438.3(SPTAN1):c.3161G>A (p.Arg1054His) rs561564501
NM_001130438.3(SPTAN1):c.3262G>A (p.Glu1088Lys) rs780374369
NM_001130438.3(SPTAN1):c.3519+5G>T rs915019884
NM_001130438.3(SPTAN1):c.3579+3_3579+4dup rs797046004
NM_001130438.3(SPTAN1):c.363+1G>A rs1554737064
NM_001130438.3(SPTAN1):c.3673C>T (p.Arg1225Trp) rs569997507
NM_001130438.3(SPTAN1):c.3779A>G (p.Asn1260Ser) rs552623597
NM_001130438.3(SPTAN1):c.4280G>A (p.Arg1427His) rs762216368
NM_001130438.3(SPTAN1):c.4283C>G (p.Ala1428Gly) rs143166100
NM_001130438.3(SPTAN1):c.4828C>T (p.Arg1610Trp) rs1131691643
NM_001130438.3(SPTAN1):c.511A>G (p.Ile171Val) rs771906889
NM_001130438.3(SPTAN1):c.6234C>T (p.Ala2078=) rs147132904
NM_001130438.3(SPTAN1):c.6235G>A (p.Ala2079Thr) rs377253398
NM_001130438.3(SPTAN1):c.6254T>C (p.Leu2085Pro) rs1564315528
NM_001130438.3(SPTAN1):c.6273_6274delinsTT (p.Arg2092Cys) rs796053333
NM_001130438.3(SPTAN1):c.7014-16_7014-13delinsAGGT rs796053336
NM_001130438.3(SPTAN1):c.7129G>A (p.Glu2377Lys) rs757162652
NM_001130438.3(SPTAN1):c.862G>C (p.Ala288Pro) rs796053298

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