ClinVar Miner

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

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Gene type:
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Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_152296.5(ATP1A3):c.994-20T>G rs138485069 0.01603
NM_152296.5(ATP1A3):c.2688+189T>C rs114023723 0.01416
NM_152296.5(ATP1A3):c.2688+35G>A rs79365977 0.01409
NM_152296.5(ATP1A3):c.*106T>C rs180885057 0.01288
NM_152296.5(ATP1A3):c.2264-16C>T rs149116776 0.01189
NM_152296.5(ATP1A3):c.2922-58G>A rs115062483 0.01171
NM_152296.5(ATP1A3):c.2487G>A (p.Pro829=) rs45606534 0.00759
NM_152296.5(ATP1A3):c.358-206A>T rs117516508 0.00710
NM_152296.5(ATP1A3):c.1437+212G>A rs148845143 0.00483
NM_152296.5(ATP1A3):c.6+351C>G rs112446548 0.00394
NM_152296.5(ATP1A3):c.154-5C>G rs191645384 0.00188
NM_152296.5(ATP1A3):c.1943+12A>T rs201197776 0.00146
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.1438-36G>A rs199810814 0.00076
NM_152296.5(ATP1A3):c.*315G>A rs571857150 0.00073
NM_152296.5(ATP1A3):c.2653G>A (p.Val885Ile) rs149600313 0.00058
NM_152296.5(ATP1A3):c.2264-29C>T rs200137979 0.00055
NM_152296.5(ATP1A3):c.1387C>T (p.Arg463Cys) rs150785666 0.00050
NM_152296.5(ATP1A3):c.994-3C>G rs377256877 0.00046
NM_152296.5(ATP1A3):c.725-52T>A rs374815666 0.00041
NM_152296.5(ATP1A3):c.3013+134C>T rs560065605 0.00036
NM_152296.5(ATP1A3):c.1503C>T (p.Pro501=) rs143904999 0.00027
NM_152296.5(ATP1A3):c.94-21C>T rs139990019 0.00027
NM_152296.5(ATP1A3):c.1192+6C>T rs367771319 0.00026
NM_152296.5(ATP1A3):c.1193-4C>G rs200111818 0.00023
NM_152296.5(ATP1A3):c.*72A>G rs186061886 0.00022
NM_152296.5(ATP1A3):c.1695C>T (p.Asp565=) rs375255226 0.00021
NM_152296.5(ATP1A3):c.756C>T (p.Gly252=) rs150070299 0.00021
NM_152296.5(ATP1A3):c.2856G>A (p.Thr952=) rs148292376 0.00017
NM_152296.5(ATP1A3):c.2419-7C>T rs187436315 0.00016
NM_152296.5(ATP1A3):c.1500C>T (p.Ala500=) rs146606627 0.00013
NM_152296.5(ATP1A3):c.2493G>A (p.Thr831=) rs374157034 0.00013
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.2616C>A (p.Asn872Lys) rs782057287 0.00010
NM_152296.5(ATP1A3):c.1131A>G (p.Thr377=) rs143242360 0.00009
NM_152296.5(ATP1A3):c.1968C>T (p.His656=) rs142297106 0.00009
NM_152296.5(ATP1A3):c.191G>A (p.Arg64Gln) rs201573515 0.00006
NM_152296.5(ATP1A3):c.2886C>T (p.Pro962=) rs141412861 0.00006
NM_152296.5(ATP1A3):c.753G>A (p.Thr251=) rs782459932 0.00006
NM_152296.5(ATP1A3):c.2325G>A (p.Pro775=) rs150943961 0.00005
NM_152296.5(ATP1A3):c.858C>T (p.Thr286=) rs368998149 0.00005
NM_152296.5(ATP1A3):c.1017G>A (p.Lys339=) rs140106872 0.00004
NM_152296.5(ATP1A3):c.1134C>T (p.Val378=) rs180710845 0.00004
NM_152296.5(ATP1A3):c.1438-10C>T rs200271372 0.00004
NM_152296.5(ATP1A3):c.1527C>T (p.Ser509=) rs199625170 0.00004
NM_152296.5(ATP1A3):c.1821C>T (p.Thr607=) rs782381694 0.00004
NM_152296.5(ATP1A3):c.2439G>A (p.Ala813=) rs189555627 0.00004
NM_152296.5(ATP1A3):c.243G>A (p.Lys81=) rs782433549 0.00004
NM_152296.5(ATP1A3):c.472-5C>G rs372041397 0.00004
NM_152296.5(ATP1A3):c.2004C>T (p.Ile668=) rs782209649 0.00003
NM_152296.5(ATP1A3):c.2419-6G>A rs180749411 0.00003
NM_152296.5(ATP1A3):c.994-9G>A rs201175414 0.00003
NM_152296.5(ATP1A3):c.1215G>A (p.Ser405=) rs374534881 0.00002
NM_152296.5(ATP1A3):c.156T>C (p.Gly52=) rs1213410717 0.00002
NM_152296.5(ATP1A3):c.207A>T (p.Ala69=) rs200616931 0.00002
NM_152296.5(ATP1A3):c.2154C>T (p.Ala718=) rs782463652 0.00002
NM_152296.5(ATP1A3):c.2277C>T (p.Phe759=) rs782305663 0.00002
NM_152296.5(ATP1A3):c.2676C>T (p.Tyr892=) rs782625641 0.00002
NM_152296.5(ATP1A3):c.2689-11C>T rs782509039 0.00002
NM_152296.5(ATP1A3):c.2973C>T (p.Tyr991=) rs372919447 0.00002
NM_152296.5(ATP1A3):c.729G>A (p.Thr243=) rs374578592 0.00002
NM_152296.5(ATP1A3):c.741G>C (p.Val247=) rs767234141 0.00002
NM_152296.5(ATP1A3):c.*299G>A rs546192339 0.00001
NM_152296.5(ATP1A3):c.1164C>T (p.His388=) rs201446077 0.00001
NM_152296.5(ATP1A3):c.1206C>T (p.Asp402=) rs572012327 0.00001
NM_152296.5(ATP1A3):c.1839G>A (p.Thr613=) rs376852509 0.00001
NM_152296.5(ATP1A3):c.219G>A (p.Pro73=) rs567997976 0.00001
NM_152296.5(ATP1A3):c.2748C>T (p.Ile916=) rs782390447 0.00001
NM_152296.5(ATP1A3):c.315C>T (p.Tyr105=) rs782717865 0.00001
NM_152296.5(ATP1A3):c.363C>T (p.Tyr121=) rs373180830 0.00001
NM_152296.5(ATP1A3):c.381G>A (p.Ala127=) rs782313754 0.00001
NM_152296.5(ATP1A3):c.472-10C>T rs1318002472 0.00001
NM_152296.5(ATP1A3):c.750C>T (p.Ala250=) rs1555864916 0.00001
NM_152296.5(ATP1A3):c.1260C>G (p.Arg420=) rs113909283
NM_152296.5(ATP1A3):c.1323G>A (p.Ala441=) rs34578730
NM_152296.5(ATP1A3):c.1356G>A (p.Leu452=) rs1599718944
NM_152296.5(ATP1A3):c.1437+322C>T rs74488471
NM_152296.5(ATP1A3):c.1503C>G (p.Pro501=)
NM_152296.5(ATP1A3):c.2095-5_2095-4insCCCTTACCCTGCA rs782804502
NM_152296.5(ATP1A3):c.2264-107_2264-106dup rs1168002399
NM_152296.5(ATP1A3):c.2543-6T>A rs1599705282
NM_152296.5(ATP1A3):c.2772G>C (p.Leu924=)
NM_152296.5(ATP1A3):c.6+522TG[25] rs4060828
NM_152296.5(ATP1A3):c.666T>A (p.Thr222=) rs2217342
NM_152296.5(ATP1A3):c.7-4G>A rs375990668
NM_152296.5(ATP1A3):c.909C>G (p.Leu303=) rs782266448

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