List of variants in gene ATP1A2 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.3035-119A>G	rs114964592	0.03415
NM_000702.4(ATP1A2):c.1461+91G>C	rs17846712	0.02765
NM_000702.4(ATP1A2):c.178-79G>A	rs114734823	0.01365
NM_000702.4(ATP1A2):c.2840+36G>A	rs111331208	0.01293
NM_000702.4(ATP1A2):c.2943-75C>G	rs372451075	0.00303
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=)	rs138826759	0.00235
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn)	rs55858252	0.00211
NM_000702.4(ATP1A2):c.178-21C>T	rs199660548	0.00076
NM_000702.4(ATP1A2):c.1470C>T (p.Ile490=)	rs111405592	0.00044
NM_000702.4(ATP1A2):c.1652-18C>A	rs372842016	0.00015
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=)	rs139022921	0.00007
NM_000702.4(ATP1A2):c.1083G>A (p.Ala361=)	rs778171140	0.00001
NM_000702.4(ATP1A2):c.1332C>T (p.Asp444=)	rs765455081	0.00001
NM_000702.4(ATP1A2):c.1652-6C>A	rs768543626
NM_000702.4(ATP1A2):c.1652-7C>A	rs200102433

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.