ClinVar Miner

List of variants in gene OTOG reported by EGL Genetic Diagnostics, Eurofins Clinical Diagnostics

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Total variants: 37
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HGVS dbSNP
NM_001277269.1(OTOG):c.1321C>T (p.Arg441Trp) rs199968574
NM_001277269.1(OTOG):c.2421G>T (p.Gly807=) rs564595203
NM_001277269.1(OTOG):c.2434G>A (p.Asp812Asn) rs141010212
NM_001277269.1(OTOG):c.2693C>T (p.Thr898Met) rs113688475
NM_001277269.1(OTOG):c.2904-3C>T rs565665118
NM_001277269.1(OTOG):c.2907G>A (p.Val969=) rs539784682
NM_001277269.1(OTOG):c.4049G>A (p.Arg1350Gln) rs767859660
NM_001277269.1(OTOG):c.4123G>C (p.Ala1375Pro) rs7934079
NM_001277269.1(OTOG):c.4663G>A (p.Ala1555Thr) rs545740473
NM_001277269.1(OTOG):c.4762A>G (p.Thr1588Ala) rs531217323
NM_001277269.1(OTOG):c.486A>G (p.Thr162=) rs779238030
NM_001277269.1(OTOG):c.4871G>A (p.Arg1624His) rs189248390
NM_001277269.1(OTOG):c.5271C>A (p.Leu1757=) rs193083374
NM_001277269.1(OTOG):c.6217G>A (p.Val2073Met) rs748497956
NM_001277269.1(OTOG):c.6285G>T (p.Val2095=) rs774355599
NM_001277269.1(OTOG):c.6441C>T (p.Thr2147=) rs187255209
NM_001277269.1(OTOG):c.6611G>T (p.Gly2204Val) rs536834261
NM_001277269.1(OTOG):c.6703G>A (p.Val2235Met) rs572886375
NM_001277269.1(OTOG):c.6715A>G (p.Lys2239Glu) rs1554978000
NM_001277269.1(OTOG):c.6816G>A (p.Glu2272=) rs1311411933
NM_001277269.1(OTOG):c.6929G>A (p.Arg2310His) rs142799217
NM_001277269.1(OTOG):c.7304-7T>A rs911853347
NM_001277269.1(OTOG):c.7546G>A (p.Ala2516Thr) rs548278514
NM_001277269.1(OTOG):c.7686C>T (p.Ile2562=) rs187445787
NM_001277269.1(OTOG):c.7729+1G>A rs548496846
NM_001277269.1(OTOG):c.7778C>T (p.Ala2593Val) rs114417076
NM_001277269.1(OTOG):c.7903G>A (p.Asp2635Asn) rs183470913
NM_001277269.1(OTOG):c.8031C>T (p.Cys2677=) rs200809116
NM_001277269.1(OTOG):c.8248C>T (p.Arg2750Trp) rs755224664
NM_001277269.1(OTOG):c.8578-8C>T rs182750732
NM_001277269.1(OTOG):c.8698C>T (p.Gln2900Ter) rs1565133807
NM_001277269.1(OTOG):c.94G>A (p.Gly32Ser) rs565203765
NM_001277269.1(OTOG):c.973C>A (p.Pro325Thr) rs777809121
NM_001277269.2(OTOG):c.[6110C>T] rs61736002
NM_001277269.2(OTOG):c.[7667G>A] rs76461792
NM_001292063.2(OTOG):c.600CTT[1] (p.Phe202del) rs753906203
NM_001292063.2(OTOG):c.7481-5_7482dup rs1295062471

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