List of variants in gene OPA1 reported as likely benign for not specified

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

Total variants: 34

Download table as spreadsheet

HGVS	dbSNP
NM_015560.2(OPA1):c.-10C>T	rs775614028
NM_015560.2(OPA1):c.-11C>G	rs568049951
NM_015560.2(OPA1):c.1212+10T>C	rs200114656
NM_015560.2(OPA1):c.1212+9A>G	rs759086025
NM_015560.2(OPA1):c.1705+17A>G	rs749368763
NM_015560.2(OPA1):c.1706-19A>C	rs1057522968
NM_015560.2(OPA1):c.1771-21_1771-18delACTT	rs765277368
NM_015560.2(OPA1):c.182A>G (p.Gln61Arg)	rs558532319
NM_015560.2(OPA1):c.1847+7A>G	rs767488490
NM_015560.2(OPA1):c.1863A>G (p.Gln621=)	rs773826671
NM_015560.2(OPA1):c.1923G>A (p.Ala641=)	rs138114609
NM_015560.2(OPA1):c.205C>G (p.Pro69Ala)	rs750775588
NM_015560.2(OPA1):c.2064G>A (p.Pro688=)	rs768448865
NM_015560.2(OPA1):c.2167-19C>A	rs77355463
NM_015560.2(OPA1):c.2276-13T>A	rs773828534
NM_015560.2(OPA1):c.2276-4dup	rs761286590
NM_015560.2(OPA1):c.2355+13A>G	rs371943802
NM_015560.2(OPA1):c.239A>G (p.Tyr80Cys)
NM_015560.2(OPA1):c.2427T>C (p.Leu809=)	rs145999595
NM_015560.2(OPA1):c.2647A>G (p.Ile883Val)	rs149866497
NM_015560.2(OPA1):c.2707+15G>C	rs199763700
NM_015560.2(OPA1):c.2715A>G (p.Arg905=)	rs144898877
NM_015560.2(OPA1):c.2808G>C (p.Ala936=)	rs117475774
NM_015560.2(OPA1):c.32+14C>T	rs201927764
NM_015560.2(OPA1):c.534A>G (p.Leu178=)	rs758901451
NM_015560.2(OPA1):c.565G>A (p.Glu189Lys)	rs569675223
NM_015560.2(OPA1):c.6-13T>C	rs1243357575
NM_015560.2(OPA1):c.625-5527G>T	rs373326620
NM_015560.2(OPA1):c.679-4G>A	rs377043223
NM_015560.2(OPA1):c.70A>G (p.Ile24Val)	rs201520438
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.871-8G>T	rs367618769

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.