ClinVar Miner

List of variants in gene ATP1A2 reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000702.4(ATP1A2):c.*2259T>A rs3747625 0.21907
NM_000702.4(ATP1A2):c.*1026A>G rs2070704 0.21701
NM_000702.4(ATP1A2):c.*1095T>A rs56199408 0.21691
NM_000702.4(ATP1A2):c.*1629T>C rs1046995 0.21688
NM_000702.4(ATP1A2):c.*748C>T rs2070703 0.21637
NM_000702.4(ATP1A2):c.*746C>T rs62620182 0.21625
NM_000702.4(ATP1A2):c.*589G>C rs2070702 0.20323
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=) rs1063125 0.18737
NM_000702.4(ATP1A2):c.3034+14C>T rs41288127 0.13198
NM_000702.4(ATP1A2):c.*686G>A rs55843060 0.12135
NM_000702.4(ATP1A2):c.*1547G>T rs55845795 0.10469
NM_000702.4(ATP1A2):c.*1548C>T rs56003400 0.10464
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=) rs17846715 0.09239
NM_000702.4(ATP1A2):c.*1280G>A rs4656884 0.05620
NM_000702.4(ATP1A2):c.*621A>G rs12077973 0.03640
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=) rs17846714 0.03612
NM_000702.4(ATP1A2):c.*253C>T rs78930771 0.03411
NM_000702.4(ATP1A2):c.*546G>A rs62621782 0.03409
NM_000702.4(ATP1A2):c.1652-11C>G rs17846713 0.03261
NM_000702.4(ATP1A2):c.2961C>T (p.Cys987=) rs74123254 0.02590
NM_000702.4(ATP1A2):c.*682T>C rs60949592 0.02374
NM_000702.4(ATP1A2):c.*1780G>A rs74123255 0.02185
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=) rs61734529 0.02067
NM_000702.4(ATP1A2):c.*703G>A rs57902482 0.01488
NM_000702.4(ATP1A2):c.*1284C>T rs78507938 0.01486
NM_000702.4(ATP1A2):c.*72G>A rs2070701 0.00728
NM_000702.4(ATP1A2):c.*1781C>T rs116744472 0.00548
NM_000702.4(ATP1A2):c.-48C>G rs41265761 0.00401
NM_000702.4(ATP1A2):c.2943-15C>T rs111510835 0.00344
NM_000702.4(ATP1A2):c.*932T>C rs183455719 0.00339
NM_000702.4(ATP1A2):c.*1000T>G rs116194737 0.00242
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=) rs138826759 0.00235
NM_000702.4(ATP1A2):c.2115+14C>T rs200854586 0.00168
NM_000702.4(ATP1A2):c.*1355C>T rs190096000 0.00166
NM_000702.4(ATP1A2):c.*1212G>C rs558677583 0.00121
NM_000702.4(ATP1A2):c.*86G>A rs368064571 0.00099
NM_000702.4(ATP1A2):c.*482A>C rs373029091 0.00097
NM_000702.4(ATP1A2):c.2563+4C>T rs3747626 0.00088
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766 0.00075
NM_000702.4(ATP1A2):c.2751G>A (p.Thr917=) rs146839867 0.00069
NM_000702.4(ATP1A2):c.*142A>G rs117680524 0.00035
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=) rs537472446 0.00029
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=) rs148929192 0.00026
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=) rs374749325 0.00021
NM_000702.4(ATP1A2):c.*15G>A rs187737212 0.00019
NM_000702.4(ATP1A2):c.194G>T (p.Arg65Leu) rs187733403 0.00019
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566 0.00018
NM_000702.4(ATP1A2):c.1582G>A (p.Asp528Asn) rs374501280 0.00009
NM_000702.4(ATP1A2):c.2564-8A>G rs554846350 0.00009
NM_000702.4(ATP1A2):c.2412C>T (p.Ile804=) rs143969080 0.00008
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=) rs139022921 0.00007
NM_000702.4(ATP1A2):c.969C>T (p.Ile323=) rs28716941 0.00005
NM_000702.4(ATP1A2):c.151C>T (p.Arg51Cys) rs747283283 0.00002
NM_000702.4(ATP1A2):c.1572G>A (p.Glu524=) rs775192056 0.00001
NM_000702.4(ATP1A2):c.2563+15G>A rs528454399 0.00001
NM_000702.4(ATP1A2):c.2877G>A (p.Thr959=) rs200127278 0.00001
NM_000702.4(ATP1A2):c.*1000T>A rs116194737
NM_000702.4(ATP1A2):c.*1211C>A rs62621216
NM_000702.4(ATP1A2):c.*1496del rs138196662
NM_000702.4(ATP1A2):c.13-11_13-8del rs373796693
NM_000702.4(ATP1A2):c.1652-7C>A rs200102433

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