ClinVar Miner

List of variants reported as 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: 97
Download table as spreadsheet
HGVS dbSNP
NM_000702.4(ATP1A2):c.*1000T>A rs116194737
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.*1212G>C rs558677583
NM_000702.4(ATP1A2):c.*1280G>A rs4656884
NM_000702.4(ATP1A2):c.*1284C>T rs78507938
NM_000702.4(ATP1A2):c.*1355C>T rs190096000
NM_000702.4(ATP1A2):c.*142A>G rs117680524
NM_000702.4(ATP1A2):c.*1496del rs138196662
NM_000702.4(ATP1A2):c.*1547G>T rs55845795
NM_000702.4(ATP1A2):c.*1548C>T rs56003400
NM_000702.4(ATP1A2):c.*15G>A
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.*482A>C
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.*86G>A
NM_000702.4(ATP1A2):c.*932T>C rs183455719
NM_000702.4(ATP1A2):c.-48C>G rs41265761
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=) rs1063125
NM_000702.4(ATP1A2):c.13-11_13-8del rs373796693
NM_000702.4(ATP1A2):c.151C>T (p.Arg51Cys)
NM_000702.4(ATP1A2):c.1572G>A (p.Glu524=) rs775192056
NM_000702.4(ATP1A2):c.1582G>A (p.Asp528Asn) rs374501280
NM_000702.4(ATP1A2):c.1652-11C>G rs17846713
NM_000702.4(ATP1A2):c.1652-7C>A rs200102433
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=) rs17846714
NM_000702.4(ATP1A2):c.193C>T (p.Arg65Trp) rs121918619
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.2115+14C>T rs200854586
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=) rs374749325
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=) rs139022921
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=) rs17846715
NM_000702.4(ATP1A2):c.2412C>T (p.Ile804=) rs143969080
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=) rs537472446
NM_000702.4(ATP1A2):c.2563+15G>A
NM_000702.4(ATP1A2):c.2563+4C>T rs3747626
NM_000702.4(ATP1A2):c.2564-8A>G rs554846350
NM_000702.4(ATP1A2):c.2751G>A (p.Thr917=) rs146839867
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.2967C>T (p.Phe989=) rs138826759
NM_000702.4(ATP1A2):c.3034+14C>T rs41288127
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=) rs148929192
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.4(ATP1A2):c.969C>T (p.Ile323=) rs28716941
NM_152296.5(ATP1A3):c.*106T>C rs180885057
NM_152296.5(ATP1A3):c.*236T>C rs199854166
NM_152296.5(ATP1A3):c.*247C>T
NM_152296.5(ATP1A3):c.*315G>A rs571857150
NM_152296.5(ATP1A3):c.*39C>G rs919390
NM_152296.5(ATP1A3):c.1080G>A (p.Thr360=) rs370511776
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.1387C>T (p.Arg463Cys) rs150785666
NM_152296.5(ATP1A3):c.147T>C (p.Cys49=) rs376960579
NM_152296.5(ATP1A3):c.1500C>T (p.Ala500=) rs146606627
NM_152296.5(ATP1A3):c.1527C>T (p.Ser509=) rs199625170
NM_152296.5(ATP1A3):c.153+7C>T rs782082118
NM_152296.5(ATP1A3):c.154-5C>G rs191645384
NM_152296.5(ATP1A3):c.1605C>T (p.Leu535=)
NM_152296.5(ATP1A3):c.1695C>T (p.Asp565=) rs375255226
NM_152296.5(ATP1A3):c.1943+12A>T rs201197776
NM_152296.5(ATP1A3):c.1974C>T (p.Thr658=) rs145869619
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.2367G>A (p.Pro789=) rs372737275
NM_152296.5(ATP1A3):c.2419-7C>T rs187436315
NM_152296.5(ATP1A3):c.2439G>A (p.Ala813=) rs189555627
NM_152296.5(ATP1A3):c.2487G>A (p.Pro829=) rs45606534
NM_152296.5(ATP1A3):c.2559C>T (p.Leu853=)
NM_152296.5(ATP1A3):c.2610C>T (p.Pro870=) rs35272495
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.666T>G (p.Thr222=) rs2217342
NM_152296.5(ATP1A3):c.816G>A (p.Thr272=) rs149898088
NM_152296.5(ATP1A3):c.994-3C>G rs377256877

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