ClinVar Miner

List of variants in gene OPA1 reported as benign

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP
NC_000003.12:g.193593206T>A
NM_001354663.2(OPA1):c.-260_-243del rs863224140
NM_015560.2(OPA1):c.*1031A>T rs114606850
NM_015560.2(OPA1):c.*1113C>T rs12630
NM_015560.2(OPA1):c.*1343A>G rs1056366
NM_015560.2(OPA1):c.*1425G>A rs117826024
NM_015560.2(OPA1):c.*1610C>A rs73069785
NM_015560.2(OPA1):c.*2092C>T rs1056390
NM_015560.2(OPA1):c.*2115G>A rs144079165
NM_015560.2(OPA1):c.*220A>G rs76421015
NM_015560.2(OPA1):c.*2286T>C rs115575058
NM_015560.2(OPA1):c.*2344A>G rs1056392
NM_015560.2(OPA1):c.*2391T>C rs11719309
NM_015560.2(OPA1):c.*2408A>G rs73069788
NM_015560.2(OPA1):c.*283A>G rs1061648
NM_015560.2(OPA1):c.*2873A>T rs10419
NM_015560.2(OPA1):c.*2993C>A rs143991575
NM_015560.2(OPA1):c.*3027A>G rs56329083
NM_015560.2(OPA1):c.*376A>G rs142349183
NM_015560.2(OPA1):c.*560T>C rs7643844
NM_015560.2(OPA1):c.*623G>A rs146468889
NM_015560.2(OPA1):c.1071A>G (p.Ala357=) rs150807064
NM_015560.2(OPA1):c.1137T>G (p.Pro379=) rs139861334
NM_015560.2(OPA1):c.1177A>C (p.Arg393=) rs149752576
NM_015560.2(OPA1):c.1212+10T>C rs200114656
NM_015560.2(OPA1):c.1443+295G>A rs11916478
NM_015560.2(OPA1):c.1444-179G>A rs2291373
NM_015560.2(OPA1):c.1589+106G>A rs34222475
NM_015560.2(OPA1):c.1589+265A>G rs115569671
NM_015560.2(OPA1):c.1608A>C (p.Ala536=) rs78767626
NM_015560.2(OPA1):c.1770+16T>G rs9831772
NM_015560.2(OPA1):c.1770+3A>G rs398124300
NM_015560.2(OPA1):c.1884A>G (p.Val628=) rs73069703
NM_015560.2(OPA1):c.1923G>A (p.Ala641=) rs138114609
NM_015560.2(OPA1):c.2014-81G>T rs75116447
NM_015560.2(OPA1):c.2109T>C (p.Ala703=) rs9851685
NM_015560.2(OPA1):c.2167-19C>A rs77355463
NM_015560.2(OPA1):c.2256G>T (p.Leu752=) rs148047706
NM_015560.2(OPA1):c.2276-234G>A rs28457829
NM_015560.2(OPA1):c.2276-98T>C rs34558265
NM_015560.2(OPA1):c.2427T>C (p.Leu809=) rs145999595
NM_015560.2(OPA1):c.2496+306C>T rs79665962
NM_015560.2(OPA1):c.253C>T (p.Arg85Cys) rs372435892
NM_015560.2(OPA1):c.254G>A (p.Arg85His) rs35630194
NM_015560.2(OPA1):c.2613+11C>G rs111688935
NM_015560.2(OPA1):c.2707+15G>C rs199763700
NM_015560.2(OPA1):c.2707+178C>T rs11928971
NM_015560.2(OPA1):c.2715A>G (p.Arg905=) rs144898877
NM_015560.2(OPA1):c.2796C>T (p.Arg932=) rs35540805
NM_015560.2(OPA1):c.2808G>A (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.2818+206C>T rs13070791
NM_015560.2(OPA1):c.2818+207A>G rs13070610
NM_015560.2(OPA1):c.2819-126T>C rs35661865
NM_015560.2(OPA1):c.2819-250G>A rs6776228
NM_015560.2(OPA1):c.2819-4A>G rs184273607
NM_015560.2(OPA1):c.321G>A (p.Ser107=) rs117888848
NM_015560.2(OPA1):c.420G>T (p.Val140=) rs35801538
NM_015560.2(OPA1):c.43C>A (p.Gln15Lys) rs75414918
NM_015560.2(OPA1):c.448+50A>G rs377239493
NM_015560.2(OPA1):c.449-21A>G rs75213840
NM_015560.2(OPA1):c.473G>A (p.Ser158Asn) rs7624750
NM_015560.2(OPA1):c.530G>T (p.Ser177Ile) rs150279202
NM_015560.2(OPA1):c.556+178G>T rs10937593
NM_015560.2(OPA1):c.557-19T>C rs3772393
NM_015560.2(OPA1):c.557-233T>C rs9832709
NM_015560.2(OPA1):c.575C>T (p.Ala192Val) rs34307082
NM_015560.2(OPA1):c.624+296G>A rs9817704
NM_015560.2(OPA1):c.625-5451G>A rs143918255
NM_015560.2(OPA1):c.625-5528C>T rs114348597
NM_015560.2(OPA1):c.756C>T (p.Asp252=) rs147242797
NM_015560.2(OPA1):c.784-11A>C rs376681712
NM_015560.2(OPA1):c.784-12_784-11insTA rs544490050
NM_015560.2(OPA1):c.870+32T>C rs10451941
NM_015560.2(OPA1):c.870+37A>C rs76253392
NM_015560.2(OPA1):c.871-8G>T rs367618769
NM_015560.2(OPA1):c.88C>T (p.Leu30=) rs185976555
NM_130837.3(OPA1):c.*228A>G
NM_130837.3(OPA1):c.1035+4T>C rs166850
NM_130837.3(OPA1):c.1293C>T (p.Thr431=)
NM_130837.3(OPA1):c.1682-16del
NM_130837.3(OPA1):c.2521-16T>A
NM_130837.3(OPA1):c.678+13G>C

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