ClinVar Miner

List of variants in gene OTOG reported as uncertain significance

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Total variants: 110
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HGVS dbSNP
NM_001277269.1(OTOG):c.1078G>A (p.Ala360Thr) rs191354103
NM_001277269.1(OTOG):c.1099C>T (p.Pro367Ser) rs1057520124
NM_001277269.1(OTOG):c.1220A>C (p.Gln407Pro) rs876657936
NM_001277269.1(OTOG):c.1389C>A (p.Phe463Leu) rs189947237
NM_001277269.1(OTOG):c.14C>T (p.Ala5Val) rs1018902503
NM_001277269.1(OTOG):c.1582C>T (p.Arg528Cys) rs755375116
NM_001277269.1(OTOG):c.1829G>A (p.Arg610His) rs1032491736
NM_001277269.1(OTOG):c.1876C>T (p.Arg626Trp) rs201183725
NM_001277269.1(OTOG):c.1991+4C>A rs757779986
NM_001277269.1(OTOG):c.2020C>T (p.Pro674Ser) rs547173007
NM_001277269.1(OTOG):c.2312C>T (p.Ala771Val) rs876657937
NM_001277269.1(OTOG):c.2330-7A>G rs200998174
NM_001277269.1(OTOG):c.2421G>T (p.Gly807=) rs564595203
NM_001277269.1(OTOG):c.2693C>T (p.Thr898Met) rs113688475
NM_001277269.1(OTOG):c.2819G>A (p.Cys940Tyr) rs1309976795
NM_001277269.1(OTOG):c.2903+6T>G rs906307749
NM_001277269.1(OTOG):c.2904-3C>T rs565665118
NM_001277269.1(OTOG):c.2907G>A (p.Val969=) rs539784682
NM_001277269.1(OTOG):c.2921C>T (p.Ser974Leu) rs750521452
NM_001277269.1(OTOG):c.2947G>A (p.Ala983Thr) rs897016393
NM_001277269.1(OTOG):c.2975G>C (p.Arg992Pro) rs876657938
NM_001277269.1(OTOG):c.328+4A>C rs535970426
NM_001277269.1(OTOG):c.3371A>G (p.Asn1124Ser) rs571215839
NM_001277269.1(OTOG):c.3395T>C (p.Leu1132Pro) rs757588809
NM_001277269.1(OTOG):c.3474G>A (p.Met1158Ile) rs767774116
NM_001277269.1(OTOG):c.3562-12G>C rs749205983
NM_001277269.1(OTOG):c.3704C>T (p.Thr1235Ile) rs938096068
NM_001277269.1(OTOG):c.371C>G (p.Ala124Gly) rs545257884
NM_001277269.1(OTOG):c.4009C>T (p.Arg1337Cys) rs557335789
NM_001277269.1(OTOG):c.4048C>T (p.Arg1350Trp) rs61734125
NM_001277269.1(OTOG):c.4049G>A (p.Arg1350Gln) rs767859660
NM_001277269.1(OTOG):c.4096C>A (p.Pro1366Thr) rs1554974319
NM_001277269.1(OTOG):c.4165C>T (p.Arg1389Cys) rs764931529
NM_001277269.1(OTOG):c.4183C>T (p.Arg1395Cys) rs566689671
NM_001277269.1(OTOG):c.4192G>A (p.Asp1398Asn) rs876657939
NM_001277269.1(OTOG):c.433G>A (p.Gly145Ser) rs186893662
NM_001277269.1(OTOG):c.4624C>G (p.Leu1542Val) rs766929865
NM_001277269.1(OTOG):c.4677G>T (p.Glu1559Asp) rs764159927
NM_001277269.1(OTOG):c.4762A>G (p.Thr1588Ala) rs531217323
NM_001277269.1(OTOG):c.4806G>T (p.Arg1602Ser) rs147052893
NM_001277269.1(OTOG):c.4856C>T (p.Ser1619Leu) rs867891665
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.4877C>T (p.Pro1626Leu) rs897939885
NM_001277269.1(OTOG):c.5027A>T (p.His1676Leu) rs1427538566
NM_001277269.1(OTOG):c.530C>A (p.Thr177Asn) rs1396310498
NM_001277269.1(OTOG):c.5381T>C (p.Leu1794Pro) rs61744602
NM_001277269.1(OTOG):c.5416C>T (p.Arg1806Cys) rs1246889104
NM_001277269.1(OTOG):c.6073C>T (p.Arg2025Cys) rs757086717
NM_001277269.1(OTOG):c.6215G>A (p.Arg2072His) rs188527711
NM_001277269.1(OTOG):c.6215G>T (p.Arg2072Leu) rs188527711
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.6329-3C>G rs201371081
NM_001277269.1(OTOG):c.636_638CTT[1] (p.Phe214del) rs753906203
NM_001277269.1(OTOG):c.6386C>T (p.Ala2129Val) rs535700451
NM_001277269.1(OTOG):c.6441C>T (p.Thr2147=) rs187255209
NM_001277269.1(OTOG):c.6551G>A (p.Arg2184His) rs555068328
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.7003C>T (p.Arg2335Trp) rs755149839
NM_001277269.1(OTOG):c.7033G>A (p.Val2345Met) rs188832359
NM_001277269.1(OTOG):c.7045G>C (p.Val2349Leu) rs540794663
NM_001277269.1(OTOG):c.7081A>G (p.Ile2361Val) rs191722806
NM_001277269.1(OTOG):c.7183G>A (p.Gly2395Arg) rs866627770
NM_001277269.1(OTOG):c.7297A>G (p.Lys2433Glu) rs876657941
NM_001277269.1(OTOG):c.7304-7T>A rs911853347
NM_001277269.1(OTOG):c.7400C>A (p.Thr2467Asn) rs1554979068
NM_001277269.1(OTOG):c.7459G>C (p.Gly2487Arg) rs771765463
NM_001277269.1(OTOG):c.7546G>A (p.Ala2516Thr) rs548278514
NM_001277269.1(OTOG):c.7570C>T (p.Arg2524Cys) rs533820347
NM_001277269.1(OTOG):c.7694G>C (p.Arg2565Pro) rs563003848
NM_001277269.1(OTOG):c.7729+1G>A rs548496846
NM_001277269.1(OTOG):c.7778C>T (p.Ala2593Val) rs114417076
NM_001277269.1(OTOG):c.7846C>T (p.Arg2616Cys) rs876657944
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.8074G>A (p.Glu2692Lys) rs758935605
NM_001277269.1(OTOG):c.8161G>A (p.Asp2721Asn) rs189910531
NM_001277269.1(OTOG):c.8248C>T (p.Arg2750Trp) rs755224664
NM_001277269.1(OTOG):c.8381C>T (p.Thr2794Met) rs188322721
NM_001277269.1(OTOG):c.8512C>T (p.Arg2838Cys) rs191662816
NM_001277269.1(OTOG):c.8577+5G>A rs754883697
NM_001277269.1(OTOG):c.8689C>T (p.Arg2897Cys) rs185641221
NM_001277269.1(OTOG):c.8698C>T (p.Gln2900Ter) rs1565133807
NM_001277269.1(OTOG):c.919G>A (p.Val307Met) rs186310325
NM_001277269.1(OTOG):c.935A>G (p.His312Arg) rs189159426
NM_001277269.1(OTOG):c.94G>A (p.Gly32Ser) rs565203765
NM_001277269.1(OTOG):c.952G>A (p.Ala318Thr) rs553079779
NM_001277269.1(OTOG):c.973C>A (p.Pro325Thr) rs777809121
NM_001277269.1(OTOG):c.974C>T (p.Pro325Leu) rs767555421
NM_001277269.2(OTOG):c.2149A>G (p.Thr717Ala)
NM_001277269.2(OTOG):c.3089G>A (p.Cys1030Tyr)
NM_001277269.2(OTOG):c.320C>G (p.Ala107Gly)
NM_001277269.2(OTOG):c.3776G>A (p.Ser1259Asn)
NM_001277269.2(OTOG):c.401C>T (p.Thr134Ile)
NM_001277269.2(OTOG):c.4198_4215del (p.Lys1400_Ala1405del) rs876657940
NM_001277269.2(OTOG):c.5468C>T (p.Ala1823Val)
NM_001277269.2(OTOG):c.5954C>T (p.Thr1985Met)
NM_001277269.2(OTOG):c.7517-5_7518dup rs1295062471
NM_001277269.2(OTOG):c.7759G>A (p.Glu2587Lys)
NM_001277269.2(OTOG):c.800C>T (p.Ser267Leu)
NM_001277269.2(OTOG):c.8054_8055delinsAT (p.Ala2685Asp) rs876657945
NM_001277269.2(OTOG):c.8362C>T (p.Arg2788Cys)
NM_001277269.2(OTOG):c.[3719C>T] rs117005078
NM_001277269.2(OTOG):c.[421G>A] rs552304627
NM_001277269.2(OTOG):c.[6110C>T] rs61736002

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