ClinVar Miner

List of variants in gene OTOG reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_001292063.2(OTOG):c.4087G>C (p.Ala1363Pro) rs7934079 0.76845
NM_001292063.2(OTOG):c.2038T>C (p.Ser680Pro) rs7106548 0.47894
NM_001292063.2(OTOG):c.4904C>T (p.Pro1635Leu) rs2041028 0.42330
NM_001292063.2(OTOG):c.5804C>T (p.Thr1935Met) rs7111528 0.39131
NM_001292063.2(OTOG):c.2340G>A (p.Pro780=) rs4757548 0.37391
NM_001292063.2(OTOG):c.2561+14G>A rs4756902 0.37182
NM_001292063.2(OTOG):c.8241C>T (p.Cys2747=) rs10832824 0.35674
NM_001292063.2(OTOG):c.8364G>C (p.Leu2788=) rs2023483 0.35618
NM_001292063.2(OTOG):c.2561+10G>A rs4756901 0.33002
NM_001292063.2(OTOG):c.2719G>A (p.Ala907Thr) rs2355466 0.32233
NM_001292063.2(OTOG):c.8690G>C (p.Trp2897Ser) rs11024357 0.19620
NM_001292063.2(OTOG):c.7480+11A>T rs12277962 0.15041
NM_001292063.2(OTOG):c.3408+15C>T rs7936484 0.13858
NM_001292063.2(OTOG):c.3188G>A (p.Arg1063Gln) rs11024333 0.13789
NM_001292063.2(OTOG):c.1087A>T (p.Thr363Ser) rs7130190 0.13498
NM_001292063.2(OTOG):c.917C>A (p.Ala306Asp) rs61611064 0.12907
NM_001292063.2(OTOG):c.8213G>A (p.Arg2738Gln) rs12422210 0.11601
NM_001292063.2(OTOG):c.7645C>T (p.Leu2549=) rs11024350 0.11420
NM_001292063.2(OTOG):c.148C>G (p.Gln50Glu) rs76186800 0.11414
NM_001292063.2(OTOG):c.237C>T (p.Ser79=) rs11823045 0.09978
NM_001292063.2(OTOG):c.3234C>A (p.Thr1078=) rs875696 0.05453
NM_001292063.2(OTOG):c.1940C>T (p.Thr647Met) rs7112749 0.04971
NM_001292063.2(OTOG):c.3299C>T (p.Ala1100Val) rs7936324 0.04354
NM_001292063.2(OTOG):c.3350C>T (p.Pro1117Leu) rs7936354 0.04257
NM_001292063.2(OTOG):c.7894+8C>T rs11024353 0.03832
NM_001292063.2(OTOG):c.1158G>A (p.Ala386=) rs61731248 0.03769
NM_001292063.2(OTOG):c.7062T>C (p.Ser2354=) rs7114549 0.03608
NM_001292063.2(OTOG):c.7400G>A (p.Arg2467His) rs61743165 0.03602
NM_001292063.2(OTOG):c.7535G>A (p.Arg2512His) rs114242958 0.03332
NM_001292063.2(OTOG):c.688G>A (p.Ala230Thr) rs61910753 0.02905
NM_001292063.2(OTOG):c.8262C>T (p.Phe2754=) rs61730948 0.02228
NM_001292063.2(OTOG):c.769G>A (p.Val257Ile) rs61978648 0.02169
NM_001292063.2(OTOG):c.2274C>T (p.Arg758=) rs16934404 0.02154
NM_001292063.2(OTOG):c.8490G>C (p.Lys2830Asn) rs61997203 0.01716
NM_001292063.2(OTOG):c.7330G>A (p.Gly2444Ser) rs61745322 0.01656
NM_001292063.2(OTOG):c.2772C>T (p.His924=) rs61910692 0.01477
NM_001292063.2(OTOG):c.292+10A>T rs141597314 0.01457
NM_001292063.2(OTOG):c.2739G>A (p.Ser913=) rs55881341 0.01235
NM_001292063.2(OTOG):c.94+37G>A rs111425080 0.01215
NM_001292063.2(OTOG):c.3423C>T (p.Leu1141=) rs7122875 0.00974
NM_001292063.2(OTOG):c.5768T>C (p.Met1923Thr) rs61732913 0.00944
NM_001292063.2(OTOG):c.2512G>C (p.Gly838Arg) rs61734214 0.00925
NM_001292063.2(OTOG):c.3096C>T (p.Asn1032=) rs75133799 0.00891
NM_001292063.2(OTOG):c.6293-7C>T rs143985593 0.00862
NM_001292063.2(OTOG):c.6775G>A (p.Ala2259Thr) rs116503251 0.00835
NM_001292063.2(OTOG):c.4606C>T (p.Leu1536Phe) rs117380920 0.00806
NM_001292063.2(OTOG):c.996+9C>A rs147843540 0.00730
NM_001292063.2(OTOG):c.5235C>A (p.Leu1745=) rs193083374 0.00701
NM_001292063.2(OTOG):c.1797G>A (p.Arg599=) rs73418068 0.00690
NM_001292063.2(OTOG):c.21G>A (p.Ala7=) rs149500671 0.00685
NM_001292063.2(OTOG):c.5828C>T (p.Thr1943Met) rs75677194 0.00673
NM_001292063.2(OTOG):c.3351G>A (p.Pro1117=) rs146781877 0.00639
NM_001292063.2(OTOG):c.6326T>C (p.Val2109Ala) rs182000850 0.00608
NM_001292063.2(OTOG):c.1215T>C (p.Thr405=) rs73418062 0.00603
NM_001292063.2(OTOG):c.8542-8C>T rs182750732 0.00565
NM_001292063.2(OTOG):c.385+7C>T rs139222878 0.00540
NM_001292063.2(OTOG):c.7825C>A (p.Gln2609Lys) rs61995750 0.00485
NM_001292063.2(OTOG):c.7045A>G (p.Ile2349Val) rs191722806 0.00457
NM_001292063.2(OTOG):c.3525+10C>A rs113275496 0.00451
NM_001292063.2(OTOG):c.8035C>T (p.Arg2679Cys) rs567966154 0.00428
NM_001292063.2(OTOG):c.3674G>A (p.Arg1225His) rs116947228 0.00420
NM_001292063.2(OTOG):c.2967G>A (p.Pro989=) rs11024331 0.00392
NM_001292063.2(OTOG):c.1059C>T (p.Val353=) rs74921579 0.00385
NM_001292063.2(OTOG):c.534C>T (p.Ser178=) rs61995706 0.00371
NM_001292063.2(OTOG):c.3683C>T (p.Pro1228Leu) rs117005078 0.00338
NM_001292063.2(OTOG):c.843G>A (p.Lys281=) rs570688276 0.00312
NM_001292063.2(OTOG):c.2398G>A (p.Asp800Asn) rs141010212 0.00287
NM_001292063.2(OTOG):c.1104-4A>C rs149163390 0.00257
NM_001292063.2(OTOG):c.4022G>A (p.Arg1341Gln) rs145689709 0.00242
NM_001292063.2(OTOG):c.7867G>A (p.Asp2623Asn) rs183470913 0.00242
NM_001292063.2(OTOG):c.1340A>G (p.Asn447Ser) rs115772736 0.00238
NM_001292063.2(OTOG):c.1397T>G (p.Phe466Cys) rs147355325 0.00232
NM_001292063.2(OTOG):c.6074C>T (p.Ala2025Val) rs61736002 0.00229
NM_001292063.2(OTOG):c.6893G>A (p.Arg2298His) rs142799217 0.00211
NM_001292063.2(OTOG):c.5549C>G (p.Pro1850Arg) rs376684690 0.00210
NM_001292063.2(OTOG):c.8369G>A (p.Arg2790His) rs117315845 0.00188
NM_001292063.2(OTOG):c.3618C>T (p.Ser1206=) rs143393149 0.00179
NM_001292063.2(OTOG):c.311A>G (p.Asn104Ser) rs534942001 0.00140
NM_001292063.2(OTOG):c.1050C>T (p.His350=) rs575344158 0.00053
NM_001292063.2(OTOG):c.7935+11G>A rs188456860 0.00050
NM_001292063.2(OTOG):c.1051G>A (p.Ala351Thr) rs756177290 0.00011
NM_001292063.2(OTOG):c.1353C>A (p.Phe451Leu) rs189947237
NM_001292063.2(OTOG):c.2723G>T (p.Arg908Leu) rs144060182
NM_001292063.2(OTOG):c.3289-8C>G rs12792504
NM_001292063.2(OTOG):c.5459C>G (p.Ala1820Gly) rs1003490
NM_001292063.2(OTOG):c.5459C>T (p.Ala1820Val) rs1003490
NM_001292063.2(OTOG):c.8191-12C>A rs11828989

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