ClinVar Miner

List of variants in gene OTOF reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_194248.3(OTOF):c.4767C>T (p.Arg1589=) rs80356578 0.01544
NM_194248.3(OTOF):c.2215-19C>G rs111033427 0.00434
NM_194248.3(OTOF):c.2215-80T>C rs143141993 0.00268
NM_194248.3(OTOF):c.245G>A (p.Arg82His) rs149766574 0.00237
NM_194248.3(OTOF):c.4980C>T (p.Asp1660=) rs149549554 0.00164
NM_194248.3(OTOF):c.4091G>T (p.Gly1364Val) rs138037294 0.00155
NM_194248.3(OTOF):c.1530C>T (p.Ile510=) rs150452778 0.00093
NM_194248.3(OTOF):c.3384C>T (p.Pro1128=) rs145151677 0.00093
NM_194248.3(OTOF):c.2908C>T (p.Arg970Cys) rs140613217 0.00081
NM_194248.3(OTOF):c.2407-17C>T rs111706333 0.00055
NM_194248.3(OTOF):c.1020C>T (p.Asp340=) rs138250704 0.00048
NM_194248.3(OTOF):c.4483C>A (p.Arg1495=) rs147321712 0.00048
NM_194248.3(OTOF):c.80-5C>T rs531034566 0.00040
NM_194248.3(OTOF):c.1708C>T (p.Leu570=) rs138474867 0.00039
NM_194248.3(OTOF):c.3679C>A (p.Arg1227=) rs111033478 0.00027
NM_194248.3(OTOF):c.2664G>A (p.Thr888=) rs112230402 0.00026
NM_194248.3(OTOF):c.1035C>T (p.Tyr345=) rs138885901 0.00016
NM_194248.3(OTOF):c.5331C>T (p.Asp1777=) rs141082575 0.00016
NM_194248.3(OTOF):c.446C>T (p.Thr149Met) rs140454738 0.00015
NM_194323.3(OTOF):c.3600C>T (p.Ile1200=) rs145899319 0.00014
NM_194248.3(OTOF):c.2180A>G (p.Asn727Ser) rs200654171 0.00012
NM_194248.3(OTOF):c.234C>T (p.Ile78=) rs201753818 0.00010
NM_194248.3(OTOF):c.447G>A (p.Thr149=) rs151257291 0.00006
NM_194248.3(OTOF):c.5610C>T (p.Thr1870=) rs141119917 0.00005
NM_194248.3(OTOF):c.1045+12C>T rs761253981 0.00003
NM_194248.3(OTOF):c.660G>A (p.Ser220=) rs745785393 0.00003
NM_194248.3(OTOF):c.828C>T (p.Cys276=) rs111033447 0.00003
NM_194248.3(OTOF):c.2688G>A (p.Lys896=) rs886038757 0.00002
NM_194248.3(OTOF):c.4782C>T (p.Ile1594=) rs765847178 0.00002
NM_194248.3(OTOF):c.1522G>A (p.Val508Met)
NM_194248.3(OTOF):c.1965C>A (p.Pro655=) rs886038756
NM_194248.3(OTOF):c.231C>T (p.Leu77=)
NM_194248.3(OTOF):c.2505G>A (p.Leu835=)
NM_194248.3(OTOF):c.5673C>T (p.Pro1891=)

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