ClinVar Miner

List of variants in gene OPA1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP
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.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.1884A>G (p.Val628=) rs73069703
NM_015560.2(OPA1):c.2014-81G>T rs75116447
NM_015560.2(OPA1):c.2109T>C (p.Ala703=) rs9851685
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.2496+306C>T rs79665962
NM_015560.2(OPA1):c.2613+11C>G rs111688935
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.473G>A (p.Ser158Asn) rs7624750
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.625-5528C>T rs114348597
NM_015560.2(OPA1):c.88C>T (p.Leu30=) rs185976555
NM_130837.3(OPA1):c.1035+4T>C rs166850

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.