ClinVar Miner

List of variants in gene OTOF reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_194248.3(OTOF):c.*220C>T
NM_194248.3(OTOF):c.*372C>T rs56025829
NM_194248.3(OTOF):c.*650C>A rs57941637
NM_194248.3(OTOF):c.-120G>T rs114469860
NM_194248.3(OTOF):c.-67G>A rs13422586
NM_194248.3(OTOF):c.1185C>T (p.Thr395=) rs61739877
NM_194248.3(OTOF):c.145C>T (p.Arg49Trp) rs61746568
NM_194248.3(OTOF):c.1926C>T (p.Asn642=) rs72853741
NM_194248.3(OTOF):c.2022C>T (p.Asp674=) rs13004993
NM_194248.3(OTOF):c.2025G>A (p.Glu675=) rs61746988
NM_194248.3(OTOF):c.2317C>T (p.Arg773Cys) rs80356569
NM_194248.3(OTOF):c.2381G>A (p.Arg794His) rs80356592
NM_194248.3(OTOF):c.2401G>T (p.Glu801Ter) rs75624587
NM_194248.3(OTOF):c.2402A>T (p.Glu801Val) rs61739883
NM_194248.3(OTOF):c.2452C>T (p.Arg818Trp) rs2272070
NM_194248.3(OTOF):c.2464C>T (p.Arg822Trp) rs80356570
NM_194248.3(OTOF):c.2613C>T (p.Leu871=) rs2272068
NM_194248.3(OTOF):c.2703G>A (p.Ser901=) rs4997760
NM_194248.3(OTOF):c.2829C>T (p.Gly943=) rs73920285
NM_194248.3(OTOF):c.2908C>T (p.Arg970Cys) rs140613217
NM_194248.3(OTOF):c.3608A>G (p.Asn1203Ser) rs61740776
NM_194248.3(OTOF):c.3751T>G (p.Cys1251Gly) rs41288773
NM_194248.3(OTOF):c.4629-9C>T rs72853726
NM_194248.3(OTOF):c.4677G>A (p.Val1559=) rs2272071
NM_194248.3(OTOF):c.4767C>T (p.Arg1589=) rs80356578
NM_194248.3(OTOF):c.5026C>T (p.Arg1676Cys) rs139767460
NM_194248.3(OTOF):c.5063C>T (p.Thr1688Met) rs111033393
NM_194248.3(OTOF):c.509+10A>G rs76712142
NM_194248.3(OTOF):c.5655C>T (p.Arg1885=) rs45442103
NM_194248.3(OTOF):c.945G>A (p.Lys315=) rs41288779

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