ClinVar Miner

List of variants reported as likely benign for alternating hemiplegia by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 61
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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
NM_152296.5(ATP1A3):c.*106T>C rs180885057
NM_152296.5(ATP1A3):c.*236T>C rs199854166
NM_152296.5(ATP1A3):c.*298C>T rs781980860
NM_152296.5(ATP1A3):c.*315G>A rs571857150
NM_152296.5(ATP1A3):c.-64A>G rs373531937
NM_152296.5(ATP1A3):c.1192+6C>T rs367771319
NM_152296.5(ATP1A3):c.1281G>A (p.Gln427=) rs116979196
NM_152296.5(ATP1A3):c.1323G>A (p.Ala441=) rs34578730
NM_152296.5(ATP1A3):c.147T>C (p.Cys49=) rs376960579
NM_152296.5(ATP1A3):c.1527C>T (p.Ser509=) rs199625170
NM_152296.5(ATP1A3):c.154-5C>G rs191645384
NM_152296.5(ATP1A3):c.1943+12A>T rs201197776
NM_152296.5(ATP1A3):c.207A>T (p.Ala69=) rs200616931
NM_152296.5(ATP1A3):c.2319T>C (p.Asn773=) rs61733017
NM_152296.5(ATP1A3):c.2334G>A (p.Thr778=) rs145374789
NM_152296.5(ATP1A3):c.2419-7C>T rs187436315
NM_152296.5(ATP1A3):c.2487G>A (p.Pro829=) rs45606534
NM_152296.5(ATP1A3):c.2610C>T (p.Pro870=) rs35272495
NM_152296.5(ATP1A3):c.2838C>T (p.Phe946=) rs141421692
NM_152296.5(ATP1A3):c.288C>T (p.Ile96=) rs142806181
NM_152296.5(ATP1A3):c.357C>T (p.Asn119=) rs143547136
NM_152296.5(ATP1A3):c.363C>T (p.Tyr121=) rs373180830
NM_152296.5(ATP1A3):c.6+3A>G rs369853936
NM_152296.5(ATP1A3):c.994-3C>G rs377256877

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