ClinVar Miner

List of variants in gene OTOF reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_194248.3(OTOF):c.*126G>A rs73920281
NM_194248.3(OTOF):c.1185C>T (p.Thr395=) rs61739877
NM_194248.3(OTOF):c.129C>T (p.Asp43=) rs116525289
NM_194248.3(OTOF):c.1424A>G (p.Glu475Gly) rs111033396
NM_194248.3(OTOF):c.145C>T (p.Arg49Trp) rs61746568
NM_194248.3(OTOF):c.157G>A (p.Ala53Thr) rs144915302
NM_194248.3(OTOF):c.1580-6C>T rs114260271
NM_194248.3(OTOF):c.1580-7G>T rs116430138
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.1961G>A (p.Arg654Gln) rs184605839
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.2215-155A>G rs143933877
NM_194248.3(OTOF):c.2215-19C>G rs111033427
NM_194248.3(OTOF):c.2215-77T>G rs76130130
NM_194248.3(OTOF):c.2215-80T>C rs143141993
NM_194248.3(OTOF):c.2215-83C>T rs4665855
NM_194248.3(OTOF):c.2317C>T (p.Arg773Cys) rs80356569
NM_194248.3(OTOF):c.2401_2402delinsTT (p.Glu801Leu) rs111033392
NM_194248.3(OTOF):c.244C>T (p.Arg82Cys) rs13031859
NM_194248.3(OTOF):c.245G>A (p.Arg82His) rs149766574
NM_194248.3(OTOF):c.2464C>T (p.Arg822Trp) rs80356570
NM_194248.3(OTOF):c.2512C>T (p.Leu838=) rs146139327
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.297G>A (p.Thr99=) rs397517941
NM_194248.3(OTOF):c.3076A>T (p.Arg1026Trp) rs145239283
NM_194248.3(OTOF):c.3189G>A (p.Ala1063=) rs80356573
NM_194248.3(OTOF):c.3247G>C (p.Ala1083Pro) rs80356574
NM_194248.3(OTOF):c.3470G>A (p.Arg1157Gln) rs56054534
NM_194248.3(OTOF):c.3471G>T (p.Arg1157=) rs61742191
NM_194248.3(OTOF):c.3608A>G (p.Asn1203Ser) rs61740776
NM_194248.3(OTOF):c.367G>A (p.Gly123Ser) rs116314622
NM_194248.3(OTOF):c.372A>G (p.Thr124=) rs11687696
NM_194248.3(OTOF):c.3734-10A>C rs73920284
NM_194248.3(OTOF):c.3751T>G (p.Cys1251Gly) rs41288773
NM_194248.3(OTOF):c.37C>T (p.Leu13=) rs76180450
NM_194248.3(OTOF):c.42G>A (p.Arg14=) rs6734111
NM_194248.3(OTOF):c.4332C>T (p.Thr1444=) rs149236286
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.4800-11C>T rs41286009
NM_194248.3(OTOF):c.4869C>T (p.Gly1623=) rs61744000
NM_194248.3(OTOF):c.4936C>T (p.Pro1646Ser) rs17005371
NM_194248.3(OTOF):c.4980C>T (p.Asp1660=) rs149549554
NM_194248.3(OTOF):c.5026C>T (p.Arg1676Cys) rs139767460
NM_194248.3(OTOF):c.5039G>A (p.Arg1680His) rs11893228
NM_194248.3(OTOF):c.505C>T (p.Arg169Trp) rs61744348
NM_194248.3(OTOF):c.509+10A>G rs76712142
NM_194248.3(OTOF):c.509+11G>A rs200010052
NM_194248.3(OTOF):c.5097C>T (p.Ile1699=) rs12386239
NM_194248.3(OTOF):c.51C>T (p.Gly17=) rs142333075
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.5558G>A (p.Arg1853Gln) rs111033329
NM_194248.3(OTOF):c.5655C>T (p.Arg1885=) rs45442103
NM_194248.3(OTOF):c.5742G>A (p.Leu1914=) rs141235641
NM_194248.3(OTOF):c.710+10C>T rs55639868
NM_194248.3(OTOF):c.766-3C>T rs55886964
NM_194248.3(OTOF):c.945G>A (p.Lys315=) rs41288779
NM_194248.3(OTOF):c.98G>A (p.Arg33Gln) rs56332208

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