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=) rs571886426
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.4298G>A (p.Arg1433Gln) rs778218478
NM_001277269.2(OTOG):c.8574C>T (p.Thr2858=) rs201952556
NM_001277269.2(OTOG):c.[3719C>T] rs117005078
NM_001277269.2(OTOG):c.[4058G>A] rs145689709
NM_001277269.2(OTOG):c.[6110C>T] rs61736002
NM_001292063.2(OTOG):c.1560C>T (p.Phe520=) rs1482605363
NM_001292063.2(OTOG):c.441C>T (p.His147=) rs567294014
NM_001292063.2(OTOG):c.5121T>G (p.Val1707=) rs563661860
NM_001292063.2(OTOG):c.7557G>A (p.Glu2519=) rs577246890
NM_001292063.2(OTOG):c.7800T>C (p.Cys2600=) rs1333602999
NM_001292063.2(OTOG):c.7827G>A (p.Gln2609=) rs1351651117
NM_001292063.2(OTOG):c.7962G>A (p.Glu2654=) rs976702124
NM_001292063.2(OTOG):c.8190+8G>A rs1258304711
NM_001292063.2(OTOG):c.8718C>G (p.Thr2906=) rs1195829508

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