ClinVar Miner

List of variants in gene CNGA3 studied for Achromatopsia 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NM_001079878.2(CNGA3):c.101+1G>A rs147118493
NM_001079878.2(CNGA3):c.1174C>T (p.Arg392Trp) rs137852608
NM_001079878.2(CNGA3):c.1252C>T (p.Arg418Trp) rs104893621
NM_001079878.2(CNGA3):c.1256_1258delinsAG (p.Val419fs) rs1558820471
NM_001079878.2(CNGA3):c.130_151dup (p.Ala51fs) rs1558811557
NM_001079878.2(CNGA3):c.1503G>A (p.Met501Ile) rs199655686
NM_001079878.2(CNGA3):c.1531G>A (p.Val511Met) rs104893619
NM_001079878.2(CNGA3):c.1587C>A (p.Phe529Leu) rs104893617
NM_001079878.2(CNGA3):c.1615G>A (p.Gly539Arg) rs104893615
NM_001079878.2(CNGA3):c.434C>T (p.Pro145Leu) rs104893612
NM_001079878.2(CNGA3):c.628G>A (p.Glu210Lys) rs147415641
NM_001079878.2(CNGA3):c.67C>T (p.Arg23Ter) rs777509481
NM_001079878.2(CNGA3):c.773A>G (p.Asn258Ser) rs199474697
NM_001079878.2(CNGA3):c.775C>T (p.Arg259Cys) rs104893620
NM_001079878.2(CNGA3):c.793C>T (p.Arg265Trp) rs104893613
NM_001079878.2(CNGA3):c.794G>A (p.Arg265Gln) rs104893614
NM_001079878.2(CNGA3):c.818C>G (p.Thr273Arg) rs104893616
NM_001079878.2(CNGA3):c.913G>C (p.Ala305Pro) rs146195955
NM_001079878.2(CNGA3):c.980A>G (p.His327Arg) rs780411290
NM_001298.3(CNGA3):c.778G>A (p.Asp260Asn)

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.