ClinVar Miner

List of variants in gene ATP1A3 reported as benign for not provided

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_152296.5(ATP1A3):c.666T>G (p.Thr222=) rs2217342 0.93139
NM_152296.5(ATP1A3):c.2264-170C>T rs10425063 0.73405
NM_152296.5(ATP1A3):c.*39C>G rs919390 0.69962
NM_152296.5(ATP1A3):c.2542+137T>A rs12975677 0.69748
NM_152296.5(ATP1A3):c.2820-68G>A rs4306638 0.02530
NM_152296.5(ATP1A3):c.2689-217C>A rs73051437 0.02391
NM_152296.5(ATP1A3):c.1437+76C>G rs75979328 0.02292
NM_152296.5(ATP1A3):c.6+183C>T rs114694347 0.02249
NM_152296.5(ATP1A3):c.994-295C>T rs116420327 0.02089
NM_152296.5(ATP1A3):c.*127A>C rs782239785 0.01887
NM_152296.5(ATP1A3):c.2819+164T>C rs145937694 0.01757
NM_152296.5(ATP1A3):c.2319T>C (p.Asn773=) rs61733017 0.01238
NM_152296.5(ATP1A3):c.2610C>T (p.Pro870=) rs35272495 0.00802
NM_152296.5(ATP1A3):c.2487G>A (p.Pro829=) rs45606534 0.00759
NM_152296.5(ATP1A3):c.2819+20G>A rs148592392 0.00279
NM_152296.5(ATP1A3):c.2922-33C>T rs137887337 0.00247
NM_152296.5(ATP1A3):c.2334G>A (p.Thr778=) rs145374789 0.00243
NM_152296.5(ATP1A3):c.2921+11C>T rs190570469 0.00230
NM_152296.5(ATP1A3):c.*296C>T rs149277536 0.00228
NM_152296.5(ATP1A3):c.1944-20G>T rs200665663 0.00216
NM_152296.5(ATP1A3):c.154-5C>G rs191645384 0.00188
NM_152296.5(ATP1A3):c.2976C>T (p.Asp992=) rs146199765 0.00177
NM_152296.5(ATP1A3):c.816G>A (p.Thr272=) rs149898088 0.00140
NM_152296.5(ATP1A3):c.357C>T (p.Asn119=) rs143547136 0.00108
NM_152296.5(ATP1A3):c.7-64T>C rs371478724 0.00090
NM_152296.5(ATP1A3):c.1260C>T (p.Arg420=) rs113909283 0.00080
NM_152296.5(ATP1A3):c.993+51C>T rs113311604 0.00079
NM_152296.5(ATP1A3):c.192G>A (p.Arg64=) rs146053862 0.00061
NM_152296.5(ATP1A3):c.2653G>A (p.Val885Ile) rs149600313 0.00058
NM_152296.5(ATP1A3):c.994-3C>G rs377256877 0.00046
NM_152296.5(ATP1A3):c.1193-4C>G rs200111818 0.00023
NM_152296.5(ATP1A3):c.1695C>T (p.Asp565=) rs375255226 0.00021
NM_152296.5(ATP1A3):c.2419-26C>T rs189151960 0.00018
NM_152296.5(ATP1A3):c.2419-7C>T rs187436315 0.00016
NM_152296.5(ATP1A3):c.2263+43G>A rs782672374 0.00014
NM_152296.5(ATP1A3):c.147T>C (p.Cys49=) rs376960579 0.00011
NM_152296.5(ATP1A3):c.2226C>T (p.Asp742=) rs146600566 0.00011
NM_152296.5(ATP1A3):c.288C>T (p.Ile96=) rs142806181 0.00011
NM_152296.5(ATP1A3):c.1131A>G (p.Thr377=) rs143242360 0.00009
NM_152296.5(ATP1A3):c.1776G>A (p.Ala592=) rs2288507 0.00009
NM_152296.5(ATP1A3):c.1086C>T (p.Thr362=) rs186453162 0.00007
NM_152296.5(ATP1A3):c.1281G>A (p.Gln427=) rs116979196 0.00007
NM_152296.5(ATP1A3):c.1192+3G>A rs374542368 0.00002
NM_152296.5(ATP1A3):c.207A>T (p.Ala69=) rs200616931 0.00002
NM_152296.5(ATP1A3):c.363C>T (p.Tyr121=) rs373180830 0.00001
NM_152296.5(ATP1A3):c.*247C>T rs565195548
NM_152296.5(ATP1A3):c.1323G>A (p.Ala441=) rs34578730
NM_152296.5(ATP1A3):c.2264-107dup rs1168002399
NM_152296.5(ATP1A3):c.2820-278_2820-275del rs10587805
NM_152296.5(ATP1A3):c.6+522TG[20] rs4060828
NM_152296.5(ATP1A3):c.6+522TG[21] rs4060828
NM_152296.5(ATP1A3):c.6+522TG[22] rs4060828
NM_152296.5(ATP1A3):c.6+522TG[23] rs4060828
NM_152296.5(ATP1A3):c.725-32C>A rs201351299

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