ClinVar Miner

List of variants in gene SPTAN1 reported as likely benign for not provided

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Total variants: 45
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HGVS dbSNP
NM_001130438.3(SPTAN1):c.1085+113A>G
NM_001130438.3(SPTAN1):c.1221+115T>A
NM_001130438.3(SPTAN1):c.1338C>G (p.Ser446=)
NM_001130438.3(SPTAN1):c.1357C>T (p.Leu453=)
NM_001130438.3(SPTAN1):c.1572+143A>G
NM_001130438.3(SPTAN1):c.2194-89G>A
NM_001130438.3(SPTAN1):c.2324C>T (p.Ala775Val) rs144649618
NM_001130438.3(SPTAN1):c.2343C>T (p.Ala781=) rs34084388
NM_001130438.3(SPTAN1):c.2763C>T (p.Asp921=)
NM_001130438.3(SPTAN1):c.3235C>G (p.Leu1079Val) rs559839676
NM_001130438.3(SPTAN1):c.3415-305T>C
NM_001130438.3(SPTAN1):c.3510G>A (p.Val1170=)
NM_001130438.3(SPTAN1):c.3518A>C (p.Gln1173Pro) rs141696651
NM_001130438.3(SPTAN1):c.3520-14C>G rs142682344
NM_001130438.3(SPTAN1):c.3528T>C (p.Tyr1176=)
NM_001130438.3(SPTAN1):c.3579+228A>G
NM_001130438.3(SPTAN1):c.3627+164C>T
NM_001130438.3(SPTAN1):c.3666C>T (p.Ala1222=)
NM_001130438.3(SPTAN1):c.3834C>T (p.Phe1278=)
NM_001130438.3(SPTAN1):c.3865-7C>T
NM_001130438.3(SPTAN1):c.3941G>A (p.Cys1314Tyr)
NM_001130438.3(SPTAN1):c.4027C>T (p.Arg1343Cys)
NM_001130438.3(SPTAN1):c.4153C>T (p.Arg1385Trp) rs770189298
NM_001130438.3(SPTAN1):c.4199A>T (p.Gln1400Leu) rs143108250
NM_001130438.3(SPTAN1):c.4345-14C>T
NM_001130438.3(SPTAN1):c.4479G>A (p.Ala1493=)
NM_001130438.3(SPTAN1):c.4580A>G (p.Asn1527Ser) rs145038571
NM_001130438.3(SPTAN1):c.504+157_504+158insCTCTCCAGCTCTCC
NM_001130438.3(SPTAN1):c.504+159_504+160insGC
NM_001130438.3(SPTAN1):c.504+162_504+163insCTCTAG
NM_001130438.3(SPTAN1):c.513T>C (p.Ile171=)
NM_001130438.3(SPTAN1):c.5301A>G (p.Glu1767=) rs200641770
NM_001130438.3(SPTAN1):c.5358-195A>G
NM_001130438.3(SPTAN1):c.5529A>G (p.Lys1843=)
NM_001130438.3(SPTAN1):c.5734-234G>T
NM_001130438.3(SPTAN1):c.6070-12C>T
NM_001130438.3(SPTAN1):c.6420C>T (p.Ala2140=)
NM_001130438.3(SPTAN1):c.6576+284C>T
NM_001130438.3(SPTAN1):c.6707+10_6707+12delinsTTC
NM_001130438.3(SPTAN1):c.6762+151A>C
NM_001130438.3(SPTAN1):c.6763-44G>A
NM_001130438.3(SPTAN1):c.7160+27G>A
NM_001130438.3(SPTAN1):c.7199T>C (p.Met2400Thr)
NM_001130438.3(SPTAN1):c.7390G>A (p.Ala2464Thr)
NM_001130438.3(SPTAN1):c.7414C>T (p.Arg2472Cys) rs759975874

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