ClinVar Miner

List of variants in gene OTOG reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
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.8542-8C>T rs182750732 0.00545
NM_001292063.2(OTOG):c.8416-16G>A rs146753764 0.00537
NM_001292063.2(OTOG):c.3683C>T (p.Pro1228Leu) rs117005078 0.00338
NM_001292063.2(OTOG):c.7631G>A (p.Arg2544Gln) rs76461792 0.00309
NM_001292063.2(OTOG):c.843G>A (p.Lys281=) rs570688276 0.00307
NM_001292063.2(OTOG):c.2398G>A (p.Asp800Asn) rs141010212 0.00287
NM_001292063.2(OTOG):c.899A>G (p.His300Arg) rs189159426 0.00243
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.6074C>T (p.Ala2025Val) rs61736002 0.00240
NM_001292063.2(OTOG):c.1104-4A>C rs149163390 0.00238
NM_001292063.2(OTOG):c.1340A>G (p.Asn447Ser) rs115772736 0.00238
NM_001292063.2(OTOG):c.8369G>A (p.Arg2790His) rs117315845 0.00202
NM_001292063.2(OTOG):c.5345T>C (p.Leu1782Pro) rs61744602 0.00187
NM_001292063.2(OTOG):c.1285C>T (p.Arg429Trp) rs199968574 0.00166
NM_001292063.2(OTOG):c.5252G>A (p.Arg1751His) rs185432248 0.00122
NM_001292063.2(OTOG):c.4641G>T (p.Glu1547Asp) rs764159927 0.00060
NM_001292063.2(OTOG):c.8538C>T (p.Thr2846=) rs201952556 0.00060
NM_001292063.2(OTOG):c.8646G>A (p.Leu2882=) rs542151771 0.00058
NM_001292063.2(OTOG):c.1050C>T (p.His350=) rs575344158 0.00053
NM_001292063.2(OTOG):c.8019C>T (p.Ala2673=) rs531303093 0.00050
NM_001292063.2(OTOG):c.7209C>T (p.Ser2403=) rs56236649 0.00048
NM_001292063.2(OTOG):c.8322C>T (p.Cys2774=) rs539684481 0.00048
NM_001292063.2(OTOG):c.1323C>T (p.Asp441=) rs571886426 0.00047
NM_001292063.2(OTOG):c.7866C>T (p.Pro2622=) rs200566292 0.00040
NM_001292063.2(OTOG):c.2331C>T (p.Cys777=) rs147247967 0.00036
NM_001292063.2(OTOG):c.7742C>T (p.Ala2581Val) rs114417076 0.00032
NM_001292063.2(OTOG):c.6536T>C (p.Val2179Ala) rs770039471 0.00027
NM_001292063.2(OTOG):c.540+8C>T rs1027600196 0.00018
NM_001292063.2(OTOG):c.5919G>A (p.Thr1973=) rs570611759 0.00014
NM_001292063.2(OTOG):c.2397C>T (p.Gly799=) rs779489639 0.00013
NM_001292063.2(OTOG):c.4629C>T (p.Ala1543=) rs547273913 0.00011
NM_001292063.2(OTOG):c.2736C>T (p.Leu912=) rs190031749 0.00008
NM_001292063.2(OTOG):c.5650A>G (p.Thr1884Ala) rs561598526 0.00007
NM_001292063.2(OTOG):c.5856C>T (p.Ala1952=) rs778221743 0.00007
NM_001292063.2(OTOG):c.2271C>T (p.Phe757=) rs781432242 0.00005
NM_001292063.2(OTOG):c.6075G>A (p.Ala2025=) rs562628744 0.00005
NM_001292063.2(OTOG):c.8607C>T (p.Thr2869=) rs1247864136 0.00005
NM_001292063.2(OTOG):c.6444C>T (p.His2148=) rs776163972 0.00004
NM_001292063.2(OTOG):c.7611A>C (p.Ala2537=) rs540270096 0.00004
NM_001292063.2(OTOG):c.2481C>G (p.Val827=) rs1368317019 0.00003
NM_001292063.2(OTOG):c.3684G>A (p.Pro1228=) rs755990926 0.00003
NM_001292063.2(OTOG):c.7464C>T (p.Cys2488=) rs774023506 0.00003
NM_001292063.2(OTOG):c.1830C>T (p.Asn610=) rs1354880626 0.00001
NM_001292063.2(OTOG):c.4719A>T (p.Ala1573=) rs2497531566 0.00001
NM_001292063.2(OTOG):c.5517T>C (p.Thr1839=) rs1481243061 0.00001
NM_001292063.2(OTOG):c.94+74C>T rs978749480 0.00001
NM_001292063.2(OTOG):c.2646C>T (p.Ser882=)
NM_001292063.2(OTOG):c.2723G>T (p.Arg908Leu) rs144060182
NM_001292063.2(OTOG):c.3210G>A (p.Val1070=) rs1342195087
NM_001292063.2(OTOG):c.5184C>G (p.Ala1728=) rs543256557
NM_001292063.2(OTOG):c.6120T>C (p.Cys2040=) rs777071359
NM_001292063.2(OTOG):c.6132C>T (p.Ala2044=) rs935529251
NM_001292063.2(OTOG):c.6179G>A (p.Arg2060His) rs188527711
NM_001292063.2(OTOG):c.8091C>T (p.Gly2697=) rs535312212

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