ClinVar Miner

List of variants in gene OTOG reported as likely benign by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 107
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HGVS dbSNP
NM_001277269.1(OTOG):c.1060C>T (p.Leu354=) rs876657550
NM_001277269.1(OTOG):c.1078G>A (p.Ala360Thr) rs191354103
NM_001277269.1(OTOG):c.1249+14A>C rs143302987
NM_001277269.1(OTOG):c.1321C>T (p.Arg441Trp) rs199968574
NM_001277269.1(OTOG):c.1322G>A (p.Arg441Gln) rs528799547
NM_001277269.1(OTOG):c.1379-8C>T rs876657551
NM_001277269.1(OTOG):c.1491A>G (p.Thr497=) rs1554968896
NM_001277269.1(OTOG):c.1599C>G (p.Pro533=) rs749836896
NM_001277269.1(OTOG):c.1659G>A (p.Leu553=) rs755383141
NM_001277269.1(OTOG):c.1842C>T (p.Ser614=) rs536715287
NM_001277269.1(OTOG):c.2134G>A (p.Ala712Thr) rs113745835
NM_001277269.1(OTOG):c.2330-6C>T rs201721923
NM_001277269.1(OTOG):c.2423T>C (p.Val808Ala) rs1554970485
NM_001277269.1(OTOG):c.2522+7G>A rs774905533
NM_001277269.1(OTOG):c.2523-5dup rs562652501
NM_001277269.1(OTOG):c.2597+9C>T rs528157125
NM_001277269.1(OTOG):c.2598-14G>A rs550895099
NM_001277269.1(OTOG):c.2661C>G (p.Gly887=) rs876657552
NM_001277269.1(OTOG):c.2868C>T (p.Phe956=) rs876657553
NM_001277269.1(OTOG):c.3042+11G>A rs150247729
NM_001277269.1(OTOG):c.3053A>T (p.Asp1018Val) rs551850126
NM_001277269.1(OTOG):c.3114G>A (p.Arg1038=) rs1244694943
NM_001277269.1(OTOG):c.3265A>G (p.Ile1089Val) rs56359117
NM_001277269.1(OTOG):c.328+15C>T rs876657554
NM_001277269.1(OTOG):c.3300C>T (p.His1100=) rs776482697
NM_001277269.1(OTOG):c.3396A>G (p.Leu1132=) rs779322374
NM_001277269.1(OTOG):c.3434C>T (p.Ala1145Val) rs768393908
NM_001277269.1(OTOG):c.3855G>A (p.Ala1285=) rs750862882
NM_001277269.1(OTOG):c.3975C>T (p.Ala1325=) rs1554974304
NM_001277269.1(OTOG):c.4038C>T (p.Phe1346=) rs545896255
NM_001277269.1(OTOG):c.4048C>T (p.Arg1350Trp) rs61734125
NM_001277269.1(OTOG):c.4057C>T (p.Arg1353Trp) rs200215464
NM_001277269.1(OTOG):c.407C>T (p.Pro136Leu) rs542646349
NM_001277269.1(OTOG):c.4206G>A (p.Ser1402=) rs765085598
NM_001277269.1(OTOG):c.4274G>A (p.Arg1425Gln) rs143848095
NM_001277269.1(OTOG):c.4282C>T (p.Arg1428Trp) rs559512010
NM_001277269.1(OTOG):c.4283G>A (p.Arg1428Gln) rs147318012
NM_001277269.1(OTOG):c.431C>T (p.Ala144Val) rs766172178
NM_001277269.1(OTOG):c.4663G>A (p.Ala1555Thr) rs545740473
NM_001277269.1(OTOG):c.4857G>A (p.Ser1619=) rs369768224
NM_001277269.1(OTOG):c.4862C>T (p.Pro1621Leu) rs937557181
NM_001277269.1(OTOG):c.4871G>A (p.Arg1624His) rs189248390
NM_001277269.1(OTOG):c.4902C>T (p.Val1634=) rs780581249
NM_001277269.1(OTOG):c.4932G>A (p.Thr1644=) rs143785785
NM_001277269.1(OTOG):c.495G>T (p.Gly165=) rs1554967816
NM_001277269.1(OTOG):c.5087C>T (p.Pro1696Leu) rs553479177
NM_001277269.1(OTOG):c.5256A>C (p.Pro1752=) rs959286824
NM_001277269.1(OTOG):c.5288G>A (p.Arg1763His) rs185432248
NM_001277269.1(OTOG):c.5339A>G (p.Glu1780Gly) rs876657555
NM_001277269.1(OTOG):c.5381T>C (p.Leu1794Pro) rs61744602
NM_001277269.1(OTOG):c.5503G>A (p.Gly1835Ser) rs539129544
NM_001277269.1(OTOG):c.563G>C (p.Ser188Thr) rs876657556
NM_001277269.1(OTOG):c.576+8C>T rs1027600196
NM_001277269.1(OTOG):c.5849C>T (p.Thr1950Met) rs758489218
NM_001277269.1(OTOG):c.6015G>A (p.Ser2005=) rs925237259
NM_001277269.1(OTOG):c.6042G>A (p.Pro2014=) rs554657199
NM_001277269.1(OTOG):c.6255C>T (p.Pro2085=) rs876657557
NM_001277269.1(OTOG):c.6557A>G (p.Asn2186Ser) rs368261417
NM_001277269.1(OTOG):c.6703G>A (p.Val2235Met) rs572886375
NM_001277269.1(OTOG):c.675G>T (p.Glu225Asp) rs61736015
NM_001277269.1(OTOG):c.6943C>T (p.Arg2315Cys) rs568549806
NM_001277269.1(OTOG):c.6973C>T (p.Pro2325Ser) rs543999548
NM_001277269.1(OTOG):c.7084G>A (p.Glu2362Lys) rs375080152
NM_001277269.1(OTOG):c.7389A>C (p.Gln2463His) rs145833172
NM_001277269.1(OTOG):c.7416T>A (p.Asp2472Glu) rs532385451
NM_001277269.1(OTOG):c.7497C>T (p.Cys2499=) rs530992812
NM_001277269.1(OTOG):c.7546G>A (p.Ala2516Thr) rs548278514
NM_001277269.1(OTOG):c.7578C>G (p.Leu2526=) rs752641698
NM_001277269.1(OTOG):c.7621+11C>T rs369343034
NM_001277269.1(OTOG):c.7621+12G>A rs538124093
NM_001277269.1(OTOG):c.7653G>T (p.Leu2551=) rs908026995
NM_001277269.1(OTOG):c.7729+11G>A rs976807214
NM_001277269.1(OTOG):c.7729+13C>T rs773422239
NM_001277269.1(OTOG):c.7729+14A>T rs545542156
NM_001277269.1(OTOG):c.7758C>A (p.Pro2586=) rs1260956852
NM_001277269.1(OTOG):c.7882C>T (p.Leu2628=) rs876657558
NM_001277269.1(OTOG):c.7902C>T (p.Pro2634=) rs200566292
NM_001277269.1(OTOG):c.7926C>T (p.Ser2642=) rs555614943
NM_001277269.1(OTOG):c.7995G>A (p.Glu2665=) rs762613093
NM_001277269.1(OTOG):c.8011G>A (p.Val2671Met) rs542442173
NM_001277269.1(OTOG):c.8031C>T (p.Cys2677=) rs200809116
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.8072G>A (p.Arg2691His) rs766229978
NM_001277269.1(OTOG):c.819G>T (p.Met273Ile) rs118083195
NM_001277269.1(OTOG):c.8204T>C (p.Leu2735Pro) rs180703235
NM_001277269.1(OTOG):c.8256C>T (p.Leu2752=) rs749120808
NM_001277269.1(OTOG):c.8283C>T (p.Asn2761=) rs778915475
NM_001277269.1(OTOG):c.8334C>A (p.Pro2778=) rs569159135
NM_001277269.1(OTOG):c.8358C>T (p.Cys2786=) rs539684481
NM_001277269.1(OTOG):c.8508T>C (p.Asp2836=) rs940623349
NM_001277269.1(OTOG):c.8512C>T (p.Arg2838Cys) rs191662816
NM_001277269.1(OTOG):c.8607C>T (p.Cys2869=) rs1166068398
NM_001277269.1(OTOG):c.8682G>A (p.Leu2894=) rs542151771
NM_001277269.1(OTOG):c.915C>T (p.Asp305=) rs144220847
NM_001277269.1(OTOG):c.935A>G (p.His312Arg) rs189159426
NM_001277269.1(OTOG):c.973C>A (p.Pro325Thr) rs777809121
NM_001277269.2(OTOG):c.16T>C (p.Ser6Pro) rs773298682
NM_001277269.2(OTOG):c.3213C>T (p.Val1071=) rs184126223
NM_001277269.2(OTOG):c.3219A>C (p.Thr1073=) rs780180476
NM_001277269.2(OTOG):c.6128C>T (p.Thr2043Ile) rs545321215
NM_001277269.2(OTOG):c.6863C>T (p.Thr2288Ile) rs569603083
NM_001277269.2(OTOG):c.7245C>T (p.Ser2415=) rs56236649
NM_001277269.2(OTOG):c.7458C>T (p.Phe2486=) rs983539027
NM_001277269.2(OTOG):c.7803G>A (p.Thr2601=) rs748617558
NM_001277269.2(OTOG):c.[7667G>A] rs76461792
NM_001292063.1(OTOG):c.94+75G>T rs550807341

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