ClinVar Miner

List of variants in gene ATP1A2 reported as likely benign for alternating hemiplegia

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP
NM_000702.4(ATP1A2):c.*1000T>G rs116194737
NM_000702.4(ATP1A2):c.*1026A>G rs2070704
NM_000702.4(ATP1A2):c.*1095T>A rs56199408
NM_000702.4(ATP1A2):c.*1211C>A rs62621216
NM_000702.4(ATP1A2):c.*1280G>A rs4656884
NM_000702.4(ATP1A2):c.*1284C>T rs78507938
NM_000702.4(ATP1A2):c.*142A>G rs117680524
NM_000702.4(ATP1A2):c.*1547G>T rs55845795
NM_000702.4(ATP1A2):c.*1548C>T rs56003400
NM_000702.4(ATP1A2):c.*1629T>C rs1046995
NM_000702.4(ATP1A2):c.*1780G>A rs74123255
NM_000702.4(ATP1A2):c.*1781C>T rs116744472
NM_000702.4(ATP1A2):c.*2259T>A rs3747625
NM_000702.4(ATP1A2):c.*253C>T rs78930771
NM_000702.4(ATP1A2):c.*546G>A rs62621782
NM_000702.4(ATP1A2):c.*589G>C rs2070702
NM_000702.4(ATP1A2):c.*621A>G rs12077973
NM_000702.4(ATP1A2):c.*682T>C rs60949592
NM_000702.4(ATP1A2):c.*686G>A rs55843060
NM_000702.4(ATP1A2):c.*703G>A rs57902482
NM_000702.4(ATP1A2):c.*72G>A rs2070701
NM_000702.4(ATP1A2):c.*746C>T rs62620182
NM_000702.4(ATP1A2):c.*748C>T rs2070703
NM_000702.4(ATP1A2):c.-48C>G rs41265761
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys) rs142348542
NM_000702.4(ATP1A2):c.1652-11C>G rs17846713
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=) rs17846714
NM_000702.4(ATP1A2):c.194G>T (p.Arg65Leu) rs187733403
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=) rs61734529
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=) rs17846715
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=) rs537472446
NM_000702.4(ATP1A2):c.2563+4C>T rs3747626
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.4(ATP1A2):c.2877G>A (p.Thr959=) rs200127278
NM_000702.4(ATP1A2):c.2943-15C>T rs111510835
NM_000702.4(ATP1A2):c.2961C>T (p.Cys987=) rs74123254
NM_000702.4(ATP1A2):c.3034+14C>T rs41288127

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.