ClinVar Miner

List of variants in gene OTOF reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_194248.3(OTOF):c.-120G>T rs114469860
NM_194248.3(OTOF):c.1046-92A>T
NM_194248.3(OTOF):c.129C>T (p.Asp43=) rs116525289
NM_194248.3(OTOF):c.138+28T>G
NM_194248.3(OTOF):c.145C>T (p.Arg49Trp) rs61746568
NM_194248.3(OTOF):c.158C>T (p.Ala53Val) rs1879761
NM_194248.3(OTOF):c.1723G>A (p.Val575Met) rs55676840
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.2215-83C>T rs4665855
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.2406+36G>A
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.2736G>C (p.Leu912=) rs4335905
NM_194248.3(OTOF):c.2829C>T (p.Gly943=) rs73920285
NM_194248.3(OTOF):c.328-59T>C
NM_194248.3(OTOF):c.3608A>G (p.Asn1203Ser) rs61740776
NM_194248.3(OTOF):c.372A>G (p.Thr124=) rs11687696
NM_194248.3(OTOF):c.3894+22G>A
NM_194248.3(OTOF):c.4341G>A (p.Glu1447=) rs80214437
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.4936C>T (p.Pro1646Ser) rs17005371
NM_194248.3(OTOF):c.509+10A>G rs76712142
NM_194248.3(OTOF):c.5097C>T (p.Ile1699=) rs12386239
NM_194248.3(OTOF):c.5391C>T (p.Phe1797=) rs61747275
NM_194248.3(OTOF):c.5418C>T (p.Ile1806=) rs116990436
NM_194248.3(OTOF):c.5655C>T (p.Arg1885=) rs45442103
NM_194248.3(OTOF):c.766-3C>T rs55886964
NM_194248.3(OTOF):c.945G>A (p.Lys315=) rs41288779

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