ClinVar Miner

List of variants in gene OPA1 reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
Download table as spreadsheet
HGVS dbSNP
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.*1815T>C rs570796106
NM_015560.2(OPA1):c.*1919T>A rs867799524
NM_015560.2(OPA1):c.*2092C>T rs1056390
NM_015560.2(OPA1):c.*2115G>A rs144079165
NM_015560.2(OPA1):c.*2156A>G rs886058258
NM_015560.2(OPA1):c.*220A>G rs76421015
NM_015560.2(OPA1):c.*2241A>G rs778074372
NM_015560.2(OPA1):c.*2283A>G rs886058259
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.*2416C>T rs539683627
NM_015560.2(OPA1):c.*2605_*2607delGGA rs886058260
NM_015560.2(OPA1):c.*260G>T rs886058256
NM_015560.2(OPA1):c.*2692G>A rs886058261
NM_015560.2(OPA1):c.*2694T>A rs886058262
NM_015560.2(OPA1):c.*283A>G rs1061648
NM_015560.2(OPA1):c.*2873A>T rs10419
NM_015560.2(OPA1):c.*2909A>T rs886058263
NM_015560.2(OPA1):c.*2993C>A rs143991575
NM_015560.2(OPA1):c.*3027A>G rs56329083
NM_015560.2(OPA1):c.*3147G>C rs886058264
NM_015560.2(OPA1):c.*322G>A rs886058257
NM_015560.2(OPA1):c.*376A>G rs142349183
NM_015560.2(OPA1):c.*560T>C rs7643844
NM_015560.2(OPA1):c.*56C>T rs564487151
NM_015560.2(OPA1):c.*622C>T rs750359704
NM_015560.2(OPA1):c.*623G>A rs146468889
NM_015560.2(OPA1):c.*694C>A rs190367068
NM_015560.2(OPA1):c.*863A>G rs193292545
NM_015560.2(OPA1):c.-102G>A rs886058255
NM_015560.2(OPA1):c.-8C>T rs371988066
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.1146A>G (p.Ile382Met) rs143319805
NM_015560.2(OPA1):c.1177A>C (p.Arg393=) rs149752576
NM_015560.2(OPA1):c.1572G>C (p.Gln524His) rs538099724
NM_015560.2(OPA1):c.1608A>C (p.Ala536=) rs78767626
NM_015560.2(OPA1):c.1884A>G (p.Val628=) rs73069703
NM_015560.2(OPA1):c.2109T>C (p.Ala703=) rs9851685
NM_015560.2(OPA1):c.2166+10T>C rs371096629
NM_015560.2(OPA1):c.2341C>T (p.Arg781Trp) rs190235251
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.2796C>T (p.Arg932=) rs35540805
NM_015560.2(OPA1):c.2808G>A (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.2819-4A>G rs184273607
NM_015560.2(OPA1):c.321G>A (p.Ser107=) rs117888848
NM_015560.2(OPA1):c.339C>T (p.Tyr113=) rs779836454
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.530G>T (p.Ser177Ile) rs150279202
NM_015560.2(OPA1):c.544T>C (p.Phe182Leu) rs769335936
NM_015560.2(OPA1):c.575C>T (p.Ala192Val) rs34307082
NM_015560.2(OPA1):c.599C>T (p.Ser200Phe) rs200243596
NM_015560.2(OPA1):c.70A>G (p.Ile24Val) rs201520438
NM_015560.2(OPA1):c.825C>T (p.Leu275=) rs201242590
NM_015560.2(OPA1):c.852G>A (p.Thr284=) rs758922394
NM_015560.2(OPA1):c.870+4T>C rs166850
NM_015560.2(OPA1):c.871-9T>C rs531187028
NM_130831.2(OPA1):c.420G>T (p.Val140=) rs35801538
NM_130837.2(OPA1):c.2441-4dupC rs761286590

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.