ClinVar Miner

List of variants in gene OTOF reported as likely benign for Nonsyndromic Hearing Loss, Recessive

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_194248.3(OTOF):c.*372C>T rs56025829
NM_194248.3(OTOF):c.*650C>A rs57941637
NM_194248.3(OTOF):c.*696A>G rs55744034
NM_194248.3(OTOF):c.*697G>A rs60182448
NM_194248.3(OTOF):c.*898dup rs111964688
NM_194248.3(OTOF):c.129C>T (p.Asp43=) rs116525289
NM_194248.3(OTOF):c.158C>T (p.Ala53Val) rs1879761
NM_194248.3(OTOF):c.2022C>T (p.Asp674=) rs13004993
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.244C>T (p.Arg82Cys) rs13031859
NM_194248.3(OTOF):c.2580C>G (p.Val860=) rs2272069
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.372A>G (p.Thr124=) rs11687696
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.4936C>T (p.Pro1646Ser) rs17005371
NM_194248.3(OTOF):c.509+10A>G rs76712142
NM_194248.3(OTOF):c.945G>A (p.Lys315=) rs41288779

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