ClinVar Miner

List of variants in gene ATP1A2 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_000702.4(ATP1A2):c.381+16C>T rs2820581 0.95274
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=) rs1063125 0.18359
NM_000702.4(ATP1A2):c.3034+14C>T rs41288127 0.13198
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=) rs17846715 0.09246
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=) rs17846714 0.03612
NM_000702.4(ATP1A2):c.1652-11C>G rs17846713 0.03344
NM_000702.4(ATP1A2):c.1125G>A (p.Lys375=) rs61734526 0.00323
NM_000702.4(ATP1A2):c.836G>A (p.Arg279Gln) rs373178892 0.00056
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys) rs142348542 0.00055
NM_000702.4(ATP1A2):c.1470C>T (p.Ile490=) rs111405592 0.00048
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=) rs148929192 0.00023
NM_000702.4(ATP1A2):c.2229C>T (p.Ala743=) rs138381089 0.00017
NM_000702.4(ATP1A2):c.1251G>C (p.Thr417=) rs142309356 0.00010
NM_000702.4(ATP1A2):c.1581C>G (p.Leu527=) rs371520433 0.00010
NM_000702.4(ATP1A2):c.1332C>T (p.Asp444=) rs765455081 0.00007
NM_000702.4(ATP1A2):c.1761T>C (p.Ser587=) rs199621678 0.00006
NM_000702.4(ATP1A2):c.1735A>G (p.Lys579Glu) rs535175099 0.00005
NM_000702.4(ATP1A2):c.987C>T (p.Asn329=) rs770381135 0.00005
NM_000702.4(ATP1A2):c.789G>A (p.Thr263=) rs748890267 0.00002
NM_000702.4(ATP1A2):c.1244C>T (p.Thr415Met) rs121918618 0.00001
NM_000702.4(ATP1A2):c.2636G>A (p.Arg879Gln) rs761597771 0.00001
NM_000702.4(ATP1A2):c.888C>T (p.Val296=) rs767314566 0.00001
NM_000702.4(ATP1A2):c.1112T>A (p.Ile371Asn)
NM_000702.4(ATP1A2):c.1216+1G>A
NM_000702.4(ATP1A2):c.13-11_13-8del rs373796693
NM_000702.4(ATP1A2):c.1417C>T (p.Pro473Ser)
NM_000702.4(ATP1A2):c.1816G>A (p.Ala606Thr) rs1414742926
NM_000702.4(ATP1A2):c.2285-1G>A
NM_000702.4(ATP1A2):c.2287C>T (p.Arg763Cys) rs2101995435
NM_000702.4(ATP1A2):c.2439+3G>C
NM_000702.4(ATP1A2):c.2454_2456del (p.Leu819del)
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=) rs537472446
NM_000702.4(ATP1A2):c.2496G>A (p.Gln832=)
NM_000702.4(ATP1A2):c.2553C>T (p.Tyr851=)
NM_000702.4(ATP1A2):c.262del (p.Val88fs)
NM_000702.4(ATP1A2):c.2787T>C (p.Ala929=)
NM_000702.4(ATP1A2):c.2841-20dup rs397775888
NM_000702.4(ATP1A2):c.456C>T (p.Ser152=)
NM_000702.4(ATP1A2):c.749-4G>A
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr) rs181618883
NM_000702.4(ATP1A2):c.970G>T (p.Gly324Cys)

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