ClinVar Miner

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

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Total variants: 24
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HGVS dbSNP
NM_001277269.1(OTOG):c.1321C>T (p.Arg441Trp) rs199968574
NM_001277269.1(OTOG):c.1359C>T (p.Asp453=)
NM_001277269.1(OTOG):c.2597+9C>T rs528157125
NM_001277269.1(OTOG):c.3003G>A (p.Pro1001=) rs11024331
NM_001277269.1(OTOG):c.371C>G (p.Ala124Gly) rs545257884
NM_001277269.1(OTOG):c.7389A>C (p.Gln2463His) rs145833172
NM_001277269.1(OTOG):c.7902C>T (p.Pro2634=) rs200566292
NM_001277269.1(OTOG):c.8040C>T (p.Tyr2680=) rs892246727
NM_001277269.1(OTOG):c.8058G>A (p.Pro2686=) rs753850661
NM_001277269.1(OTOG):c.915C>T (p.Asp305=) rs144220847
NM_001277269.2(OTOG):c.1596C>T (p.Phe532=)
NM_001277269.2(OTOG):c.4298G>A (p.Arg1433Gln)
NM_001277269.2(OTOG):c.477C>T (p.His159=)
NM_001277269.2(OTOG):c.5157T>G (p.Val1719=)
NM_001277269.2(OTOG):c.7593G>A (p.Glu2531=)
NM_001277269.2(OTOG):c.7836T>C (p.Cys2612=)
NM_001277269.2(OTOG):c.7863G>A (p.Gln2621=)
NM_001277269.2(OTOG):c.7998G>A (p.Glu2666=)
NM_001277269.2(OTOG):c.8226+8G>A
NM_001277269.2(OTOG):c.8574C>T (p.Thr2858=)
NM_001277269.2(OTOG):c.8754C>G (p.Thr2918=)
NM_001277269.2(OTOG):c.[3719C>T] rs117005078
NM_001277269.2(OTOG):c.[4058G>A] rs145689709
NM_001277269.2(OTOG):c.[6110C>T] rs61736002

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