ClinVar Miner

List of variants in gene SPTAN1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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Total variants: 23
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HGVS dbSNP
NM_001130438.3(SPTAN1):c.1221+11C>T rs113357847
NM_001130438.3(SPTAN1):c.1303T>G (p.Ser435Ala) rs144787939
NM_001130438.3(SPTAN1):c.1462-27T>A rs7040737
NM_001130438.3(SPTAN1):c.1511C>T (p.Ala504Val) rs148727077
NM_001130438.3(SPTAN1):c.1737C>T (p.Phe579=) rs143941068
NM_001130438.3(SPTAN1):c.2560+43G>A rs4836615
NM_001130438.3(SPTAN1):c.2560+47C>T rs4837284
NM_001130438.3(SPTAN1):c.2872-42G>A rs4307429
NM_001130438.3(SPTAN1):c.3051G>A (p.Pro1017=) rs140279996
NM_001130438.3(SPTAN1):c.3215+15_3215+16del rs551595039
NM_001130438.3(SPTAN1):c.4272C>T (p.Asp1424=) rs1554757619
NM_001130438.3(SPTAN1):c.4905+41C>G rs7024498
NM_001130438.3(SPTAN1):c.5479-41A>C rs7864187
NM_001130438.3(SPTAN1):c.5479-5G>A rs1554763238
NM_001130438.3(SPTAN1):c.5523C>T (p.Ile1841=) rs79569204
NM_001130438.3(SPTAN1):c.6280-27C>T rs3737308
NM_001130438.3(SPTAN1):c.6498C>T (p.Arg2166=) rs72758823
NM_001130438.3(SPTAN1):c.651+37A>C rs2297769
NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=) rs112955915
NM_001130438.3(SPTAN1):c.6708-47G>A rs7866175
NM_001130438.3(SPTAN1):c.6708-7C>T rs16930539
NM_001130438.3(SPTAN1):c.6960-8T>C rs140241053
NM_001130438.3(SPTAN1):c.979C>T (p.Leu327=) rs587784442

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