List of variants in gene OPA3 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 37

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.231T>C (p.Ala77=)	rs3826860	0.70508
NM_025136.4(OPA3):c.*7015G>A	rs112948303	0.04300
NM_025136.4(OPA3):c.*6394G>A	rs151030695	0.02197
NM_025136.4(OPA3):c.143-174C>T	rs34508139	0.01902
NM_025136.4(OPA3):c.*7085A>G	rs67373144	0.01608
NM_025136.4(OPA3):c.*6275T>C	rs74689727	0.01461
NM_025136.4(OPA3):c.*1760C>T	rs75401979	0.01143
NM_025136.4(OPA3):c.*4794C>T	rs114917731	0.01114
NM_025136.4(OPA3):c.*1836C>T	rs74717111	0.01070
NM_025136.4(OPA3):c.*3222C>T	rs73568980	0.00971
NM_025136.4(OPA3):c.*6294A>C	rs114655581	0.00810
NM_025136.4(OPA3):c.*1855T>C	rs146599259	0.00697
NM_025136.4(OPA3):c.*5905G>A	rs116705343	0.00675
NM_025136.4(OPA3):c.142+81T>C	rs113539314	0.00669
NM_025136.4(OPA3):c.*362T>C	rs73942919	0.00539
NM_025136.4(OPA3):c.*5365C>T	rs73568970	0.00529
NM_025136.4(OPA3):c.*6442A>G	rs76825983	0.00518
NM_025136.4(OPA3):c.*1642A>G	rs144894771	0.00484
NM_025136.4(OPA3):c.*4954C>T	rs146646433	0.00462
NM_025136.4(OPA3):c.*6208C>T	rs139798464	0.00458
NC_000019.10:g.45584961T>C	rs115153567	0.00441
NM_025136.4(OPA3):c.*2101A>T	rs139606810	0.00363
NM_025136.4(OPA3):c.*6101A>G	rs187296782	0.00363
NM_001017989.3(OPA3):c.184G>A (p.Gly62Ser)	rs140959406	0.00223
NM_025136.4(OPA3):c.537A>G (p.Lys179=)	rs140105522	0.00158
NM_025136.4(OPA3):c.*3360G>A	rs545764728	0.00156
NM_025136.4(OPA3):c.249G>C (p.Leu83=)	rs199692583	0.00080
NM_025136.4(OPA3):c.143-7C>T	rs375551151	0.00036
NM_001017989.3(OPA3):c.486C>T (p.His162=)	rs201078416	0.00022
NM_001017989.3(OPA3):c.*2A>T	rs190812374	0.00009
NM_025136.4(OPA3):c.519A>G (p.Ala173=)	rs1200579847	0.00002
NM_001017989.3(OPA3):c.414G>A (p.Ala138=)	rs566450630
NM_001017989.3(OPA3):c.454C>T (p.Leu152=)
NM_025136.4(OPA3):c.4857_4858insC
NM_025136.4(OPA3):c.6104_6105del	rs142661638
NM_025136.4(OPA3):c.*6289A>G	rs182293743
NM_025136.4(OPA3):c.289C>T (p.Leu97=)	rs755295420

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.