ClinVar Miner

List of variants in gene OTOF reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP
NM_194248.3(OTOF):c.-113G>A rs79734645
NM_194248.3(OTOF):c.-43T>A rs201812205
NM_194248.3(OTOF):c.1149G>C (p.Gly383=) rs142219516
NM_194248.3(OTOF):c.1185C>T (p.Thr395=) rs61739877
NM_194248.3(OTOF):c.1506G>A (p.Ser502=) rs199713499
NM_194248.3(OTOF):c.1708C>T (p.Leu570=) rs138474867
NM_194248.3(OTOF):c.2025G>A (p.Glu675=) rs61746988
NM_194248.3(OTOF):c.2076G>T (p.Arg692=) rs138769870
NM_194248.3(OTOF):c.2215-136C>T rs371848783
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.2317C>T (p.Arg773Cys) rs80356569
NM_194248.3(OTOF):c.234C>T (p.Ile78=)
NM_194248.3(OTOF):c.2374C>T (p.Arg792Trp) rs148532589
NM_194248.3(OTOF):c.2375G>A (p.Arg792Gln) rs144800506
NM_194248.3(OTOF):c.237G>A (p.Gly79=) rs117985483
NM_194248.3(OTOF):c.2401_2402delinsTT (p.Glu801Leu) rs111033392
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>A (p.Val860=)
NM_194248.3(OTOF):c.2580C>T (p.Val860=)
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.3384C>T (p.Pro1128=) rs145151677
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.366C>T (p.Asp122=) rs61747283
NM_194248.3(OTOF):c.367G>A (p.Gly123Ser) rs116314622
NM_194248.3(OTOF):c.3733+39C>T
NM_194248.3(OTOF):c.3734-10A>C rs73920284
NM_194248.3(OTOF):c.3751T>G (p.Cys1251Gly) rs41288773
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.4869C>T (p.Gly1623=) rs61744000
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.5103+9T>G rs1553348387
NM_194248.3(OTOF):c.5160G>A (p.Thr1720=)
NM_194248.3(OTOF):c.51C>T (p.Gly17=) rs142333075
NM_194248.3(OTOF):c.5292-9C>T rs372713647
NM_194248.3(OTOF):c.5505G>A (p.Ala1835=) rs368190044
NM_194248.3(OTOF):c.5558G>A (p.Arg1853Gln) rs111033329
NM_194248.3(OTOF):c.5694C>T (p.Asn1898=)
NM_194248.3(OTOF):c.5742G>A (p.Leu1914=) rs141235641
NM_194248.3(OTOF):c.578G>T (p.Arg193Ile) rs139779680
NM_194248.3(OTOF):c.5813+9C>T rs1328837186
NM_194248.3(OTOF):c.633G>C (p.Arg211=)
NM_194248.3(OTOF):c.710+10C>T rs55639868
NM_194248.3(OTOF):c.98G>A (p.Arg33Gln) rs56332208

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