ClinVar Miner

List of variants in gene ATP1A2 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_000702.4(ATP1A2):c.1074C>T (p.Asn358=) rs1558005822
NM_000702.4(ATP1A2):c.1284C>T (p.Arg428=) rs752479774
NM_000702.4(ATP1A2):c.1332C>T (p.Asp444=) rs765455081
NM_000702.4(ATP1A2):c.1368G>A (p.Lys456=) rs369226331
NM_000702.4(ATP1A2):c.1470C>T (p.Ile490=) rs111405592
NM_000702.4(ATP1A2):c.152G>A (p.Arg51His) rs144106169
NM_000702.4(ATP1A2):c.1710G>A (p.Thr570=) rs536168465
NM_000702.4(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.4(ATP1A2):c.1928C>G (p.Ala643Gly) rs763782107
NM_000702.4(ATP1A2):c.2136G>A (p.Thr712=) rs760213030
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=) rs138826759
NM_000702.4(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=) rs148929192
NM_000702.4(ATP1A2):c.660G>A (p.Ser220=) rs564452950
NM_000702.4(ATP1A2):c.969C>T (p.Ile323=) rs28716941

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.