ClinVar Miner

List of variants in gene ATP2A1 reported as likely benign for not specified

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_004320.6(ATP2A1):c.1167C>T (p.Tyr389=) rs41292388 0.00255
NM_004320.6(ATP2A1):c.630+16C>G rs139443632 0.00049
NM_004320.6(ATP2A1):c.2862+20G>C rs377366848 0.00047
NM_004320.6(ATP2A1):c.2862+15G>A rs373910179 0.00036
NM_004320.6(ATP2A1):c.631-17C>T rs186636950 0.00017
NM_004320.6(ATP2A1):c.-12G>A rs201334168 0.00010
NM_004320.6(ATP2A1):c.1800G>A (p.Leu600=) rs201713188 0.00006
NM_004320.6(ATP2A1):c.463+16G>A rs568872134 0.00004
NM_004320.6(ATP2A1):c.2361G>T (p.Leu787=) rs746571879 0.00003
NM_004320.6(ATP2A1):c.2706C>T (p.Ser902=) rs779046968 0.00002
NM_004320.6(ATP2A1):c.1323C>T (p.Thr441=) rs745749841 0.00001
NM_004320.6(ATP2A1):c.1389G>A (p.Ser463=) rs368170188 0.00001
NM_004320.6(ATP2A1):c.1506A>G (p.Lys502=) rs1555516670 0.00001
NM_004320.6(ATP2A1):c.2634G>A (p.Glu878=) rs763991120 0.00001
NM_004320.6(ATP2A1):c.2772G>A (p.Arg924=) rs748003836 0.00001
NM_004320.6(ATP2A1):c.450C>T (p.Ile150=) rs781369773 0.00001
NM_004320.6(ATP2A1):c.631-10C>T rs1008154815 0.00001
NM_004320.6(ATP2A1):c.-7G>A rs1555514404
NM_004320.6(ATP2A1):c.1095+11G>C rs1555515768
NM_004320.6(ATP2A1):c.114C>T (p.Leu38=) rs1057522341
NM_004320.6(ATP2A1):c.658T>C (p.Leu220=) rs1057523426

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