ClinVar Miner

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

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Gene type:
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Total variants: 57
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HGVS dbSNP
NM_001277269.1(OTOG):c.1032+9C>A rs147843540
NM_001277269.1(OTOG):c.1086C>T (p.His362=) rs575344158
NM_001277269.1(OTOG):c.1095C>T (p.Val365=) rs74921579
NM_001277269.1(OTOG):c.1251T>C (p.Thr417=) rs73418062
NM_001277269.1(OTOG):c.1322G>A (p.Arg441Gln) rs528799547
NM_001277269.1(OTOG):c.1359C>T (p.Asp453=)
NM_001277269.1(OTOG):c.1405G>A (p.Val469Met)
NM_001277269.1(OTOG):c.1608T>C (p.Cys536=) rs1257902336
NM_001277269.1(OTOG):c.1796T>C (p.Ile599Thr)
NM_001277269.1(OTOG):c.1833G>A (p.Arg611=) rs73418068
NM_001277269.1(OTOG):c.1968T>C (p.Asn656=) rs559694792
NM_001277269.1(OTOG):c.2134G>A (p.Ala712Thr) rs113745835
NM_001277269.1(OTOG):c.21G>A (p.Ala7=) rs149500671
NM_001277269.1(OTOG):c.2329+8C>T rs1027542414
NM_001277269.1(OTOG):c.2330-7A>G rs200998174
NM_001277269.1(OTOG):c.2367C>T (p.Cys789=) rs147247967
NM_001277269.1(OTOG):c.2434G>A (p.Asp812Asn) rs141010212
NM_001277269.1(OTOG):c.2499C>G (p.Thr833=) rs771404689
NM_001277269.1(OTOG):c.2759G>T (p.Arg920Leu) rs144060182
NM_001277269.1(OTOG):c.2919C>T (p.Gly973=)
NM_001277269.1(OTOG):c.3132C>T (p.Asn1044=) rs75133799
NM_001277269.1(OTOG):c.328+10A>T rs141597314
NM_001277269.1(OTOG):c.3325-8C>G rs12792504
NM_001277269.1(OTOG):c.3336G>A (p.Ala1112=)
NM_001277269.1(OTOG):c.3372T>C (p.Asn1124=) rs1465273332
NM_001277269.1(OTOG):c.3561+10C>A rs113275496
NM_001277269.1(OTOG):c.3561+37C>T
NM_001277269.1(OTOG):c.3870G>A (p.Val1290=) rs527500084
NM_001277269.1(OTOG):c.4058G>A (p.Arg1353Gln) rs145689709
NM_001277269.1(OTOG):c.4618A>T (p.Thr1540Ser) rs747022159
NM_001277269.1(OTOG):c.4642C>T (p.Leu1548Phe) rs117380920
NM_001277269.1(OTOG):c.4857G>A (p.Ser1619=) rs369768224
NM_001277269.1(OTOG):c.4902C>T (p.Val1634=) rs780581249
NM_001277269.1(OTOG):c.5256A>C (p.Pro1752=) rs959286824
NM_001277269.1(OTOG):c.5271C>A (p.Leu1757=) rs193083374
NM_001277269.1(OTOG):c.5381T>C (p.Leu1794Pro) rs61744602
NM_001277269.1(OTOG):c.5585C>G
NM_001277269.1(OTOG):c.570C>T (p.Ser190=) rs61995706
NM_001277269.1(OTOG):c.5864C>T (p.Thr1955Met) rs75677194
NM_001277269.1(OTOG):c.6160-73G>T
NM_001277269.1(OTOG):c.627T>G (p.Ala209=)
NM_001277269.1(OTOG):c.6929G>A (p.Arg2310His) rs142799217
NM_001277269.1(OTOG):c.7667G>A (p.Arg2556Gln) rs76461792
NM_001277269.1(OTOG):c.76C>T (p.Leu26=) rs947155842
NM_001277269.1(OTOG):c.7861C>A (p.Gln2621Lys) rs61995750
NM_001277269.1(OTOG):c.8071C>T (p.Arg2691Cys) rs567966154
NM_001277269.1(OTOG):c.8204T>C (p.Leu2735Pro) rs180703235
NM_001277269.1(OTOG):c.8334C>A (p.Pro2778=) rs569159135
NM_001277269.1(OTOG):c.8405G>A (p.Arg2802His) rs117315845
NM_001277269.1(OTOG):c.8463C>T (p.Ser2821=) rs1038235034
NM_001277269.1(OTOG):c.8498-55T>C
NM_001277269.1(OTOG):c.8508T>C (p.Asp2836=) rs940623349
NM_001277269.1(OTOG):c.8526G>C (p.Lys2842Asn) rs61997203
NM_001277269.1(OTOG):c.8578-8C>T rs182750732
NM_001277269.1(OTOG):c.8613C>T (p.Ser2871=) rs931856983
NM_001277269.1(OTOG):c.879G>A (p.Lys293=) rs570688276
NM_001277269.1(OTOG):c.935A>G (p.His312Arg) rs189159426

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