Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.28900756_28900758delCA645573195ATP2A1c.1940_1942del (p.Glu647del)
c.1565_1567del (p.Glu522del)
 COSMIC COSMIC
16g.28900756A>CCA395411270ATP2A1c.1940A>C (p.Glu647Ala)
c.1565A>C (p.Glu522Ala)
16g.28900756A>GCA395411271ATP2A1c.1940A>G (p.Glu647Gly)
c.1565A>G (p.Glu522Gly)
16g.28900756A>TCA395411272ATP2A1c.1940A>T (p.Glu647Val)
c.1565A>T (p.Glu522Val)
 gnomAD v4
16g.28900757G>ACA10643415ATP2A1c.1941G>A (p.Glu647=)
c.1566G>A (p.Glu522=)
 ClinVar dbSNP gnomAD v4
16g.28900757G>CCA395411274ATP2A1c.1941G>C (p.Glu647Asp)
c.1566G>C (p.Glu522Asp)
16g.28900757G=CA2215884921ATP2A1c.1941G= (p.Glu647=)
c.1566G= (p.Glu522=)
16g.28900757G>TCA395411273ATP2A1c.1941G>T (p.Glu647Asp)
c.1566G>T (p.Glu522Asp)
16g.28900758G>ACA395411275ATP2A1c.1942G>A (p.Val648Met)
c.1567G>A (p.Val523Met)
 dbSNP gnomAD v3 gnomAD v4
16g.28900758G>CCA395411277ATP2A1c.1942G>C (p.Val648Leu)
c.1567G>C (p.Val523Leu)
16g.28900758G=CA2215884925ATP2A1c.1942G= (p.Val648=)
c.1567G= (p.Val523=)
16g.28900758G>TCA395411276ATP2A1c.1942G>T (p.Val648Leu)
c.1567G>T (p.Val523Leu)
16g.28900759T>ACA395411278ATP2A1c.1943T>A (p.Val648Glu)
c.1568T>A (p.Val523Glu)
16g.28900759T>CCA395411280ATP2A1c.1943T>C (p.Val648Ala)
c.1568T>C (p.Val523Ala)
16g.28900759T>GCA395411279ATP2A1c.1943T>G (p.Val648Gly)
c.1568T>G (p.Val523Gly)
16g.28900760G>ACA494874388ATP2A1c.1944G>A (p.Val648=)
c.1569G>A (p.Val523=)
16g.28900760G>CCA494874389ATP2A1c.1944G>C (p.Val648=)
c.1569G>C (p.Val523=)
16g.28900760G>TCA494874390ATP2A1c.1944G>T (p.Val648=)
c.1569G>T (p.Val523=)
16g.28900761G>ACA395411281ATP2A1c.1945G>A (p.Ala649Thr)
c.1570G>A (p.Ala524Thr)
 dbSNP
16g.28900761G>CCA395411282ATP2A1c.1945G>C (p.Ala649Pro)
c.1570G>C (p.Ala524Pro)
16g.28900761G=CA2215884932ATP2A1c.1945G= (p.Ala649=)
c.1570G= (p.Ala524=)
16g.28900761G>TCA395411283ATP2A1c.1945G>T (p.Ala649Ser)
c.1570G>T (p.Ala524Ser)
16g.28900762C>ACA395411284ATP2A1c.1946C>A (p.Ala649Asp)
c.1571C>A (p.Ala524Asp)
16g.28900762C=CA2215884936ATP2A1c.1946C= (p.Ala649=)
c.1571C= (p.Ala524=)
16g.28900762C>GCA395411285ATP2A1c.1946C>G (p.Ala649Gly)
c.1571C>G (p.Ala524Gly)
16g.28900762C>TCA395411286ATP2A1c.1946C>T (p.Ala649Val)
c.1571C>T (p.Ala524Val)
 dbSNP gnomAD v2 gnomAD v4
16g.28900763C>ACA494874392ATP2A1c.1947C>A (p.Ala649=)
c.1572C>A (p.Ala524=)
16g.28900763C=CA2215884942ATP2A1c.1947C= (p.Ala649=)
c.1572C= (p.Ala524=)
16g.28900763C>GCA494874393ATP2A1c.1947C>G (p.Ala649=)
c.1572C>G (p.Ala524=)
 dbSNP
16g.28900763C>TCA494874391ATP2A1c.1947C>T (p.Ala649=)
c.1572C>T (p.Ala524=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900764G>ACA7987123ATP2A1c.1948G>A (p.Asp650Asn)
c.1573G>A (p.Asp525Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900764G>CCA395411287ATP2A1c.1948G>C (p.Asp650His)
c.1573G>C (p.Asp525His)
16g.28900764G=CA2215884950ATP2A1c.1948G= (p.Asp650=)
c.1573G= (p.Asp525=)
16g.28900764G>TCA7987124ATP2A1c.1948G>T (p.Asp650Tyr)
c.1573G>T (p.Asp525Tyr)
 dbSNP ExAC gnomAD v2
16g.28900765A=CA2215884952ATP2A1c.1949A= (p.Asp650=)
c.1574A= (p.Asp525=)
16g.28900765A>CCA395411288ATP2A1c.1949A>C (p.Asp650Ala)
c.1574A>C (p.Asp525Ala)
 dbSNP gnomAD v3 gnomAD v4
16g.28900765A>GCA395411289ATP2A1c.1949A>G (p.Asp650Gly)
c.1574A>G (p.Asp525Gly)
16g.28900765A>TCA395411290ATP2A1c.1949A>T (p.Asp650Val)
c.1574A>T (p.Asp525Val)
 dbSNP gnomAD v3 gnomAD v4
16g.28900766T>ACA395411291ATP2A1c.1950T>A (p.Asp650Glu)
c.1575T>A (p.Asp525Glu)
16g.28900766T>CCA494874394ATP2A1c.1950T>C (p.Asp650=)
c.1575T>C (p.Asp525=)
 dbSNP
16g.28900766T>GCA395411292ATP2A1c.1950T>G (p.Asp650Glu)
c.1575T>G (p.Asp525Glu)
16g.28900766T=CA2215884957ATP2A1c.1950T= (p.Asp650=)
c.1575T= (p.Asp525=)
16g.28900767C>ACA395411293ATP2A1c.1951C>A (p.Arg651Ser)
c.1576C>A (p.Arg526Ser)
 COSMIC COSMIC
16g.28900767C=CA2215884966ATP2A1c.1951C= (p.Arg651=)
c.1576C= (p.Arg526=)
16g.28900767C>GCA395411294ATP2A1c.1951C>G (p.Arg651Gly)
c.1576C>G (p.Arg526Gly)
 dbSNP gnomAD v4
16g.28900767C>TCA279240353ATP2A1c.1951C>T (p.Arg651Cys)
c.1576C>T (p.Arg526Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900768G>ACA7987125ATP2A1c.1952G>A (p.Arg651His)
c.1577G>A (p.Arg526His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900768G>CCA395411295ATP2A1c.1952G>C (p.Arg651Pro)
c.1577G>C (p.Arg526Pro)
16g.28900768G=CA2215884971ATP2A1c.1952G= (p.Arg651=)
c.1577G= (p.Arg526=)
16g.28900768G>TCA395411296ATP2A1c.1952G>T (p.Arg651Leu)
c.1577G>T (p.Arg526Leu)
16g.28900769C>ACA494874395ATP2A1c.1953C>A (p.Arg651=)
c.1578C>A (p.Arg526=)
 dbSNP
16g.28900769C=CA2215884978ATP2A1c.1953C= (p.Arg651=)
c.1578C= (p.Arg526=)
16g.28900769C>GCA494874396ATP2A1c.1953C>G (p.Arg651=)
c.1578C>G (p.Arg526=)
16g.28900769C>TCA7987126ATP2A1c.1953C>T (p.Arg651=)
c.1578C>T (p.Arg526=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900770G>ACA7987127ATP2A1c.1954G>A (p.Ala652Thr)
c.1579G>A (p.Ala527Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900770G>CCA395411297ATP2A1c.1954G>C (p.Ala652Pro)
c.1579G>C (p.Ala527Pro)
16g.28900770G=CA2215884985ATP2A1c.1954G= (p.Ala652=)
c.1579G= (p.Ala527=)
16g.28900770G>TCA395411298ATP2A1c.1954G>T (p.Ala652Ser)
c.1579G>T (p.Ala527Ser)
16g.28900771C>ACA395411300ATP2A1c.1955C>A (p.Ala652Asp)
c.1580C>A (p.Ala527Asp)
16g.28900771C>GCA395411301ATP2A1c.1955C>G (p.Ala652Gly)
c.1580C>G (p.Ala527Gly)
16g.28900771C>TCA395411299ATP2A1c.1955C>T (p.Ala652Val)
c.1580C>T (p.Ala527Val)
 gnomAD v4
16g.28900772C>ACA494874397ATP2A1c.1956C>A (p.Ala652=)
c.1581C>A (p.Ala527=)
16g.28900772C=CA2215884994ATP2A1c.1956C= (p.Ala652=)
c.1581C= (p.Ala527=)
16g.28900772C>GCA494874398ATP2A1c.1956C>G (p.Ala652=)
c.1581C>G (p.Ala527=)
16g.28900772C>TCA7987128ATP2A1c.1956C>T (p.Ala652=)
c.1581C>T (p.Ala527=)
 dbSNP ExAC gnomAD v2
16g.28900773T>ACA395411302ATP2A1c.1957T>A (p.Tyr653Asn)
c.1582T>A (p.Tyr528Asn)
16g.28900773T>CCA395411303ATP2A1c.1957T>C (p.Tyr653His)
c.1582T>C (p.Tyr528His)
 ClinVar
16g.28900773T>GCA395411304ATP2A1c.1957T>G (p.Tyr653Asp)
c.1582T>G (p.Tyr528Asp)
16g.28900774A=CA2215885000ATP2A1c.1958A= (p.Tyr653=)
c.1583A= (p.Tyr528=)
16g.28900774A>CCA395411305ATP2A1c.1958A>C (p.Tyr653Ser)
c.1583A>C (p.Tyr528Ser)
16g.28900774A>GCA7987129ATP2A1c.1958A>G (p.Tyr653Cys)
c.1583A>G (p.Tyr528Cys)
 dbSNP ExAC gnomAD v3 gnomAD v4
16g.28900774A>TCA395411306ATP2A1c.1958A>T (p.Tyr653Phe)
c.1583A>T (p.Tyr528Phe)
16g.28900775C>ACA395411307ATP2A1c.1959C>A (p.Tyr653Ter)
c.1584C>A (p.Tyr528Ter)
16g.28900775C>GCA395411308ATP2A1c.1959C>G (p.Tyr653Ter)
c.1584C>G (p.Tyr528Ter)
16g.28900775C>TCA494874399ATP2A1c.1959C>T (p.Tyr653=)
c.1584C>T (p.Tyr528=)
16g.28900776A>CCA395411309ATP2A1c.1960A>C (p.Thr654Pro)
c.1585A>C (p.Thr529Pro)
16g.28900776A>GCA395411310ATP2A1c.1960A>G (p.Thr654Ala)
c.1585A>G (p.Thr529Ala)
 gnomAD v4
16g.28900776A>TCA395411311ATP2A1c.1960A>T (p.Thr654Ser)
c.1585A>T (p.Thr529Ser)
16g.28900777C>ACA395411312ATP2A1c.1961C>A (p.Thr654Lys)
c.1586C>A (p.Thr529Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.28900777C=CA2215885019ATP2A1c.1961C= (p.Thr654=)
c.1586C= (p.Thr529=)
16g.28900777C>GCA395411313ATP2A1c.1961C>G (p.Thr654Arg)
c.1586C>G (p.Thr529Arg)
16g.28900777C>TCA7987130ATP2A1c.1961C>T (p.Thr654Met)
c.1586C>T (p.Thr529Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900778G>ACA7987131ATP2A1c.1962G>A (p.Thr654=)
c.1587G>A (p.Thr529=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900778G>CCA494874400ATP2A1c.1962G>C (p.Thr654=)
c.1587G>C (p.Thr529=)
 dbSNP
16g.28900778G=CA2215885025ATP2A1c.1962G= (p.Thr654=)
c.1587G= (p.Thr529=)
16g.28900778G>TCA494874401ATP2A1c.1962G>T (p.Thr654=)
c.1587G>T (p.Thr529=)
16g.28900779G>ACA395411314ATP2A1c.1963G>A (p.Gly655Ser)
c.1588G>A (p.Gly530Ser)
16g.28900779G>CCA395411315ATP2A1c.1963G>C (p.Gly655Arg)
c.1588G>C (p.Gly530Arg)
16g.28900779G>TCA395411316ATP2A1c.1963G>T (p.Gly655Cys)
c.1588G>T (p.Gly530Cys)
16g.28900780G>ACA395411319ATP2A1c.1964G>A (p.Gly655Asp)
c.1589G>A (p.Gly530Asp)
16g.28900780G>CCA395411318ATP2A1c.1964G>C (p.Gly655Ala)
c.1589G>C (p.Gly530Ala)
16g.28900780G>TCA395411317ATP2A1c.1964G>T (p.Gly655Val)
c.1589G>T (p.Gly530Val)
16g.28900781C>ACA494874402ATP2A1c.1965C>A (p.Gly655=)
c.1590C>A (p.Gly530=)
16g.28900781C=CA2215885030ATP2A1c.1965C= (p.Gly655=)
c.1590C= (p.Gly530=)
16g.28900781C>GCA494874403ATP2A1c.1965C>G (p.Gly655=)
c.1590C>G (p.Gly530=)
16g.28900781C>TCA494874404ATP2A1c.1965C>T (p.Gly655=)
c.1590C>T (p.Gly530=)
 dbSNP
16g.28900782C>ACA7987133ATP2A1c.1966C>A (p.Arg656=)
c.1591C>A (p.Arg531=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
16g.28900782C=CA2215885034ATP2A1c.1966C= (p.Arg656=)
c.1591C= (p.Arg531=)
16g.28900782C>GCA395411320ATP2A1c.1966C>G (p.Arg656Gly)
c.1591C>G (p.Arg531Gly)
16g.28900782C>TCA7987132ATP2A1c.1966C>T (p.Arg656Ter)
c.1591C>T (p.Arg531Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900783G>ACA7987134ATP2A1c.1967G>A (p.Arg656Gln)
c.1592G>A (p.Arg531Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900783G>CCA395411321ATP2A1c.1967G>C (p.Arg656Pro)
c.1592G>C (p.Arg531Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900783G=CA2215885039ATP2A1c.1967G= (p.Arg656=)
c.1592G= (p.Arg531=)
16g.28900783G>TCA7987135ATP2A1c.1967G>T (p.Arg656Leu)
c.1592G>T (p.Arg531Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900786_28900787delCA2632539976ATP2A1c.1970_1971del (p.Glu657ValfsTer8)
c.1595_1596del (p.Glu532ValfsTer8)
 gnomAD v4
16g.28900784A=CA2215885043ATP2A1c.1968A= (p.Arg656=)
c.1593A= (p.Arg531=)
16g.28900784A>CCA494874405ATP2A1c.1968A>C (p.Arg656=)
c.1593A>C (p.Arg531=)
16g.28900784A>GCA494874407ATP2A1c.1968A>G (p.Arg656=)
c.1593A>G (p.Arg531=)
 dbSNP
16g.28900784A>TCA494874406ATP2A1c.1968A>T (p.Arg656=)
c.1593A>T (p.Arg531=)
16g.28900784dupCA622162501ATP2A1c.1968dup (p.Glu657ArgfsTer9)
c.1593dup (p.Glu532ArgfsTer9)
 dbSNP gnomAD v2 gnomAD v4
16g.28900785G>ACA395411324ATP2A1c.1969G>A (p.Glu657Lys)
c.1594G>A (p.Glu532Lys)
 COSMIC
16g.28900785G>CCA395411323ATP2A1c.1969G>C (p.Glu657Gln)
c.1594G>C (p.Glu532Gln)
 dbSNP
16g.28900785G=CA2215885049ATP2A1c.1969G= (p.Glu657=)
c.1594G= (p.Glu532=)
16g.28900785G>TCA395411322ATP2A1c.1969G>T (p.Glu657Ter)
c.1594G>T (p.Glu532Ter)
16g.28900786A>CCA395411325ATP2A1c.1970A>C (p.Glu657Ala)
c.1595A>C (p.Glu532Ala)
16g.28900786A>GCA395411327ATP2A1c.1970A>G (p.Glu657Gly)
c.1595A>G (p.Glu532Gly)
16g.28900786A>TCA395411326ATP2A1c.1970A>T (p.Glu657Val)
c.1595A>T (p.Glu532Val)
16g.28900787G>ACA494874408ATP2A1c.1971G>A (p.Glu657=)
c.1596G>A (p.Glu532=)
16g.28900787G>CCA395411328ATP2A1c.1971G>C (p.Glu657Asp)
c.1596G>C (p.Glu532Asp)
 dbSNP
16g.28900787G>TCA395411329ATP2A1c.1971G>T (p.Glu657Asp)
c.1596G>T (p.Glu532Asp)
16g.28900788T>ACA395411330ATP2A1c.1972T>A (p.Phe658Ile)
c.1597T>A (p.Phe533Ile)
16g.28900788T>CCA395411331ATP2A1c.1972T>C (p.Phe658Leu)
c.1597T>C (p.Phe533Leu)
16g.28900788T>GCA395411332ATP2A1c.1972T>G (p.Phe658Val)
c.1597T>G (p.Phe533Val)
16g.28900789T>ACA395411333ATP2A1c.1973T>A (p.Phe658Tyr)
c.1598T>A (p.Phe533Tyr)
16g.28900789T>CCA395411334ATP2A1c.1973T>C (p.Phe658Ser)
c.1598T>C (p.Phe533Ser)
16g.28900789T>GCA395411335ATP2A1c.1973T>G (p.Phe658Cys)
c.1598T>G (p.Phe533Cys)
16g.28900790C>ACA395411336ATP2A1c.1974C>A (p.Phe658Leu)
c.1599C>A (p.Phe533Leu)
 ClinVar dbSNP gnomAD v2
16g.28900790C=CA2215885060ATP2A1c.1974C= (p.Phe658=)
c.1599C= (p.Phe533=)
16g.28900790C>GCA395411337ATP2A1c.1974C>G (p.Phe658Leu)
c.1599C>G (p.Phe533Leu)
 gnomAD v4
16g.28900790C>TCA7987136ATP2A1c.1974C>T (p.Phe658=)
c.1599C>T (p.Phe533=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900791G>ACA7987137ATP2A1c.1975G>A (p.Asp659Asn)
c.1600G>A (p.Asp534Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900791G>CCA395411339ATP2A1c.1975G>C (p.Asp659His)
c.1600G>C (p.Asp534His)
16g.28900791G=CA2215885080ATP2A1c.1975G= (p.Asp659=)
c.1600G= (p.Asp534=)
16g.28900791G>TCA395411338ATP2A1c.1975G>T (p.Asp659Tyr)
c.1600G>T (p.Asp534Tyr)
16g.28900792A=CA2215885087ATP2A1c.1976A= (p.Asp659=)
c.1601A= (p.Asp534=)
16g.28900792A>CCA395411340ATP2A1c.1976A>C (p.Asp659Ala)
c.1601A>C (p.Asp534Ala)
16g.28900792A>GCA395411341ATP2A1c.1976A>G (p.Asp659Gly)
c.1601A>G (p.Asp534Gly)
 ClinVar dbSNP
16g.28900792A>TCA395411342ATP2A1c.1976A>T (p.Asp659Val)
c.1601A>T (p.Asp534Val)
16g.28900793C>ACA395411343ATP2A1c.1977C>A (p.Asp659Glu)
c.1602C>A (p.Asp534Glu)
 gnomAD v4
16g.28900793C=CA2215885102ATP2A1c.1977C= (p.Asp659=)
c.1602C= (p.Asp534=)
16g.28900793C>GCA395411344ATP2A1c.1977C>G (p.Asp659Glu)
c.1602C>G (p.Asp534Glu)
 gnomAD v4
16g.28900793C>TCA494874409ATP2A1c.1977C>T (p.Asp659=)
c.1602C>T (p.Asp534=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.28900794G>ACA7987138ATP2A1c.1978G>A (p.Asp660Asn)
c.1603G>A (p.Asp535Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
16g.28900794G>CCA395411345ATP2A1c.1978G>C (p.Asp660His)
c.1603G>C (p.Asp535His)
16g.28900794G=CA2215885116ATP2A1c.1978G= (p.Asp660=)
c.1603G= (p.Asp535=)
16g.28900794G>TCA395411346ATP2A1c.1978G>T (p.Asp660Tyr)
c.1603G>T (p.Asp535Tyr)
16g.28900795A>CCA395411347ATP2A1c.1979A>C (p.Asp660Ala)
c.1604A>C (p.Asp535Ala)
16g.28900795A>GCA395411348ATP2A1c.1979A>G (p.Asp660Gly)
c.1604A>G (p.Asp535Gly)
16g.28900795A>TCA395411349ATP2A1c.1979A>T (p.Asp660Val)
c.1604A>T (p.Asp535Val)
16g.28900796C>ACA395411350ATP2A1c.1980C>A (p.Asp660Glu)
c.1605C>A (p.Asp535Glu)
16g.28900796C=CA2215885122ATP2A1c.1980C= (p.Asp660=)
c.1605C= (p.Asp535=)
16g.28900796C>GCA395411351ATP2A1c.1980C>G (p.Asp660Glu)
c.1605C>G (p.Asp535Glu)
16g.28900796C>TCA494874410ATP2A1c.1980C>T (p.Asp660=)
c.1605C>T (p.Asp535=)
 dbSNP gnomAD v4
16g.28900797C>ACA395411352ATP2A1c.1981C>A (p.Leu661Met)
c.1606C>A (p.Leu536Met)
16g.28900797C>GCA395411353ATP2A1c.1981C>G (p.Leu661Val)
c.1606C>G (p.Leu536Val)
16g.28900797C>TCA494874411ATP2A1c.1981C>T (p.Leu661=)
c.1606C>T (p.Leu536=)
16g.28900798T>ACA395411354ATP2A1c.1982T>A (p.Leu661Gln)
c.1607T>A (p.Leu536Gln)
16g.28900798T>CCA395411355ATP2A1c.1982T>C (p.Leu661Pro)
c.1607T>C (p.Leu536Pro)
16g.28900798T>GCA395411356ATP2A1c.1982T>G (p.Leu661Arg)
c.1607T>G (p.Leu536Arg)
16g.28900799G>ACA494874412ATP2A1c.1983G>A (p.Leu661=)
c.1608G>A (p.Leu536=)
 dbSNP
16g.28900799G>CCA494874413ATP2A1c.1983G>C (p.Leu661=)
c.1608G>C (p.Leu536=)
16g.28900799G=CA2215885133ATP2A1c.1983G= (p.Leu661=)
c.1608G= (p.Leu536=)
16g.28900799G>TCA494874414ATP2A1c.1983G>T (p.Leu661=)
c.1608G>T (p.Leu536=)
16g.28900800C>ACA395411357ATP2A1c.1984C>A (p.Pro662Thr)
c.1609C>A (p.Pro537Thr)
16g.28900800C=CA2215885138ATP2A1c.1984C= (p.Pro662=)
c.1609C= (p.Pro537=)
16g.28900800C>GCA395411358ATP2A1c.1984C>G (p.Pro662Ala)
c.1609C>G (p.Pro537Ala)
16g.28900800C>TCA395411359ATP2A1c.1984C>T (p.Pro662Ser)
c.1609C>T (p.Pro537Ser)
 dbSNP gnomAD v3 gnomAD v4
16g.28900803dupCA2632539998ATP2A1c.1987dup (p.Leu663ProfsTer3)
c.1612dup (p.Leu538ProfsTer3)
 gnomAD v4
16g.28900801C>ACA395411361ATP2A1c.1985C>A (p.Pro662His)
c.1610C>A (p.Pro537His)
16g.28900801C=CA2215885143ATP2A1c.1985C= (p.Pro662=)
c.1610C= (p.Pro537=)
16g.28900801C>GCA395411360ATP2A1c.1985C>G (p.Pro662Arg)
c.1610C>G (p.Pro537Arg)
16g.28900801C>TCA7987139ATP2A1c.1985C>T (p.Pro662Leu)
c.1610C>T (p.Pro537Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900802C>ACA494874415ATP2A1c.1986C>A (p.Pro662=)
c.1611C>A (p.Pro537=)
16g.28900802C>GCA494874416ATP2A1c.1986C>G (p.Pro662=)
c.1611C>G (p.Pro537=)
16g.28900802C>TCA494874417ATP2A1c.1986C>T (p.Pro662=)
c.1611C>T (p.Pro537=)
16g.28900803C>ACA395411362ATP2A1c.1987C>A (p.Leu663Met)
c.1612C>A (p.Leu538Met)
16g.28900803C=CA2215885153ATP2A1c.1987C= (p.Leu663=)
c.1612C= (p.Leu538=)
16g.28900803C>GCA7987140ATP2A1c.1987C>G (p.Leu663Val)
c.1612C>G (p.Leu538Val)
 dbSNP ExAC gnomAD v2
16g.28900803C>TCA494874418ATP2A1c.1987C>T (p.Leu663=)
c.1612C>T (p.Leu538=)
16g.28900804T>ACA395411363ATP2A1c.1988T>A (p.Leu663Gln)
c.1613T>A (p.Leu538Gln)
16g.28900804T>CCA395411364ATP2A1c.1988T>C (p.Leu663Pro)
c.1613T>C (p.Leu538Pro)
 gnomAD v4
16g.28900804T>GCA7987141ATP2A1c.1988T>G (p.Leu663Arg)
c.1613T>G (p.Leu538Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900804T=CA2215885160ATP2A1c.1988T= (p.Leu663=)
c.1613T= (p.Leu538=)
16g.28900805G>ACA494874419ATP2A1c.1989G>A (p.Leu663=)
c.1614G>A (p.Leu538=)
16g.28900805G>CCA494874420ATP2A1c.1989G>C (p.Leu663=)
c.1614G>C (p.Leu538=)
 dbSNP gnomAD v3 gnomAD v4
16g.28900805G=CA2215885166ATP2A1c.1989G= (p.Leu663=)
c.1614G= (p.Leu538=)
16g.28900805G>TCA494874421ATP2A1c.1989G>T (p.Leu663=)
c.1614G>T (p.Leu538=)
16g.28900806G>ACA7987142ATP2A1c.1990G>A (p.Ala664Thr)
c.1615G>A (p.Ala539Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900806G>CCA395411366ATP2A1c.1990G>C (p.Ala664Pro)
c.1615G>C (p.Ala539Pro)
16g.28900806G=CA2215885174ATP2A1c.1990G= (p.Ala664=)
c.1615G= (p.Ala539=)
16g.28900806G>TCA395411365ATP2A1c.1990G>T (p.Ala664Ser)
c.1615G>T (p.Ala539Ser)
16g.28900807C>ACA395411367ATP2A1c.1991C>A (p.Ala664Asp)
c.1616C>A (p.Ala539Asp)
16g.28900807C>GCA395411368ATP2A1c.1991C>G (p.Ala664Gly)
c.1616C>G (p.Ala539Gly)
16g.28900807C>TCA395411369ATP2A1c.1991C>T (p.Ala664Val)
c.1616C>T (p.Ala539Val)
16g.28900808T>ACA494874422ATP2A1c.1992T>A (p.Ala664=)
c.1617T>A (p.Ala539=)
16g.28900808T>CCA494874423ATP2A1c.1992T>C (p.Ala664=)
c.1617T>C (p.Ala539=)
 dbSNP
16g.28900808T>GCA494874424ATP2A1c.1992T>G (p.Ala664=)
c.1617T>G (p.Ala539=)
16g.28900808T=CA2215885182ATP2A1c.1992T= (p.Ala664=)
c.1617T= (p.Ala539=)
16g.28900809G>ACA395411370ATP2A1c.1993G>A (p.Glu665Lys)
c.1618G>A (p.Glu540Lys)
 gnomAD v4
16g.28900809G>CCA395411371ATP2A1c.1993G>C (p.Glu665Gln)
c.1618G>C (p.Glu540Gln)
16g.28900809G>TCA395411372ATP2A1c.1993G>T (p.Glu665Ter)
c.1618G>T (p.Glu540Ter)
16g.28900810A>CCA395411373ATP2A1c.1994A>C (p.Glu665Ala)
c.1619A>C (p.Glu540Ala)
16g.28900810A>GCA395411374ATP2A1c.1994A>G (p.Glu665Gly)
c.1619A>G (p.Glu540Gly)
16g.28900810A>TCA395411375ATP2A1c.1994A>T (p.Glu665Val)
c.1619A>T (p.Glu540Val)
16g.28900811A=CA2215885187ATP2A1c.1995A= (p.Glu665=)
c.1620A= (p.Glu540=)
16g.28900811A>CCA395411376ATP2A1c.1995A>C (p.Glu665Asp)
c.1620A>C (p.Glu540Asp)
16g.28900811A>GCA494874425ATP2A1c.1995A>G (p.Glu665=)
c.1620A>G (p.Glu540=)
 dbSNP
16g.28900811A>TCA395411377ATP2A1c.1995A>T (p.Glu665Asp)
c.1620A>T (p.Glu540Asp)
16g.28900812C>ACA395411379ATP2A1c.1996C>A (p.Gln666Lys)
c.1621C>A (p.Gln541Lys)
16g.28900812C=CA2215885191ATP2A1c.1996C= (p.Gln666=)
c.1621C= (p.Gln541=)
16g.28900812C>GCA395411380ATP2A1c.1996C>G (p.Gln666Glu)
c.1621C>G (p.Gln541Glu)
 dbSNP gnomAD v2 gnomAD v4
16g.28900812C>TCA395411378ATP2A1c.1996C>T (p.Gln666Ter)
c.1621C>T (p.Gln541Ter)
16g.28900813A>CCA395411382ATP2A1c.1997A>C (p.Gln666Pro)
c.1622A>C (p.Gln541Pro)
16g.28900813A>GCA395411381ATP2A1c.1997A>G (p.Gln666Arg)
c.1622A>G (p.Gln541Arg)
16g.28900813A>TCA395411383ATP2A1c.1997A>T (p.Gln666Leu)
c.1622A>T (p.Gln541Leu)
16g.28900814G>ACA494874426ATP2A1c.1998G>A (p.Gln666=)
c.1623G>A (p.Gln541=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.28900814G>CCA7987143ATP2A1c.1998G>C (p.Gln666His)
c.1623G>C (p.Gln541His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900814G=CA2215885205ATP2A1c.1998G= (p.Gln666=)
c.1623G= (p.Gln541=)
16g.28900814G>TCA395411384ATP2A1c.1998G>T (p.Gln666His)
c.1623G>T (p.Gln541His)
 COSMIC COSMIC
16g.28900815C>ACA494874427ATP2A1c.1999C>A (p.Arg667=)
c.1624C>A (p.Arg542=)
16g.28900815C=CA2215885212ATP2A1c.1999C= (p.Arg667=)
c.1624C= (p.Arg542=)
16g.28900815C>GCA395411385ATP2A1c.1999C>G (p.Arg667Gly)
c.1624C>G (p.Arg542Gly)
16g.28900815C>TCA7987144ATP2A1c.1999C>T (p.Arg667Trp)
c.1624C>T (p.Arg542Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
16g.28900816G>ACA7987145ATP2A1c.2000G>A (p.Arg667Gln)
c.1625G>A (p.Arg542Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900816G>CCA395411386ATP2A1c.2000G>C (p.Arg667Pro)
c.1625G>C (p.Arg542Pro)
 ClinVar gnomAD v4
16g.28900816G=CA2215885217ATP2A1c.2000G= (p.Arg667=)
c.1625G= (p.Arg542=)
16g.28900816G>TCA395411387ATP2A1c.2000G>T (p.Arg667Leu)
c.1625G>T (p.Arg542Leu)
16g.28900817G>ACA494874428ATP2A1c.2001G>A (p.Arg667=)
c.1626G>A (p.Arg542=)
16g.28900817G>CCA494874429ATP2A1c.2001G>C (p.Arg667=)
c.1626G>C (p.Arg542=)
16g.28900817G>TCA494874430ATP2A1c.2001G>T (p.Arg667=)
c.1626G>T (p.Arg542=)
16g.28900818G>ACA395411390ATP2A1c.2002G>A (p.Glu668Lys)
c.1627G>A (p.Glu543Lys)
 gnomAD v4
16g.28900818G>CCA395411388ATP2A1c.2002G>C (p.Glu668Gln)
c.1627G>C (p.Glu543Gln)
16g.28900818G>TCA395411389ATP2A1c.2002G>T (p.Glu668Ter)
c.1627G>T (p.Glu543Ter)
16g.28900819A>CCA395411391ATP2A1c.2003A>C (p.Glu668Ala)
c.1628A>C (p.Glu543Ala)
16g.28900819A>GCA395411392ATP2A1c.2003A>G (p.Glu668Gly)
c.1628A>G (p.Glu543Gly)
16g.28900819A>TCA395411393ATP2A1c.2003A>T (p.Glu668Val)
c.1628A>T (p.Glu543Val)
16g.28900820A=CA2215885222ATP2A1c.2004A= (p.Glu668=)
c.1629A= (p.Glu543=)
16g.28900820A>CCA395411394ATP2A1c.2004A>C (p.Glu668Asp)
c.1629A>C (p.Glu543Asp)
16g.28900820A>GCA494874431ATP2A1c.2004A>G (p.Glu668=)
c.1629A>G (p.Glu543=)
 dbSNP
16g.28900820A>TCA395411395ATP2A1c.2004A>T (p.Glu668Asp)
c.1629A>T (p.Glu543Asp)
16g.28900821G>ACA395411398ATP2A1c.2005G>A (p.Ala669Thr)
c.1630G>A (p.Ala544Thr)
16g.28900821G>CCA395411396ATP2A1c.2005G>C (p.Ala669Pro)
c.1630G>C (p.Ala544Pro)
16g.28900821G>TCA395411397ATP2A1c.2005G>T (p.Ala669Ser)
c.1630G>T (p.Ala544Ser)
16g.28900822C>ACA395411399ATP2A1c.2006C>A (p.Ala669Asp)
c.1631C>A (p.Ala544Asp)
 gnomAD v4
16g.28900822C>GCA395411400ATP2A1c.2006C>G (p.Ala669Gly)
c.1631C>G (p.Ala544Gly)
 gnomAD v4
16g.28900822C>TCA395411401ATP2A1c.2006C>T (p.Ala669Val)
c.1631C>T (p.Ala544Val)
16g.28900823C>ACA494874432ATP2A1c.2007C>A (p.Ala669=)
c.1632C>A (p.Ala544=)
16g.28900823C>GCA494874433ATP2A1c.2007C>G (p.Ala669=)
c.1632C>G (p.Ala544=)
 gnomAD v4
16g.28900823C>TCA494874434ATP2A1c.2007C>T (p.Ala669=)
c.1632C>T (p.Ala544=)
16g.28900824T>ACA395411402ATP2A1c.2008T>A (p.Cys670Ser)
c.1633T>A (p.Cys545Ser)
16g.28900824T>CCA395411403ATP2A1c.2008T>C (p.Cys670Arg)
c.1633T>C (p.Cys545Arg)
16g.28900824T>GCA395411404ATP2A1c.2008T>G (p.Cys670Gly)
c.1633T>G (p.Cys545Gly)
16g.28900825G>ACA395411405ATP2A1c.2009G>A (p.Cys670Tyr)
c.1634G>A (p.Cys545Tyr)
 gnomAD v4
16g.28900825G>CCA7987146ATP2A1c.2009G>C (p.Cys670Ser)
c.1634G>C (p.Cys545Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900825G=CA2215885225ATP2A1c.2009G= (p.Cys670=)
c.1634G= (p.Cys545=)
16g.28900825G>TCA395411406ATP2A1c.2009G>T (p.Cys670Phe)
c.1634G>T (p.Cys545Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900826C>ACA395411407ATP2A1c.2010C>A (p.Cys670Ter)
c.1635C>A (p.Cys545Ter)
16g.28900826C>GCA395411408ATP2A1c.2010C>G (p.Cys670Trp)
c.1635C>G (p.Cys545Trp)
16g.28900826C>TCA494874435ATP2A1c.2010C>T (p.Cys670=)
c.1635C>T (p.Cys545=)
16g.28900827C>ACA494874436ATP2A1c.2011C>A (p.Arg671=)
c.1636C>A (p.Arg546=)
 gnomAD v4
16g.28900827C=CA2215885227ATP2A1c.2011C= (p.Arg671=)
c.1636C= (p.Arg546=)
16g.28900827C>GCA395411409ATP2A1c.2011C>G (p.Arg671Gly)
c.1636C>G (p.Arg546Gly)
16g.28900827C>TCA395411410ATP2A1c.2011C>T (p.Arg671Ter)
c.1636C>T (p.Arg546Ter)
 ClinVar dbSNP gnomAD v4
16g.28900828G>ACA7987147ATP2A1c.2012G>A (p.Arg671Gln)
c.1637G>A (p.Arg546Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900828G>CCA395411412ATP2A1c.2012G>C (p.Arg671Pro)
c.1637G>C (p.Arg546Pro)
16g.28900828G=CA2215885230ATP2A1c.2012G= (p.Arg671=)
c.1637G= (p.Arg546=)
16g.28900828G>TCA395411411ATP2A1c.2012G>T (p.Arg671Leu)
c.1637G>T (p.Arg546Leu)
16g.28900829A=CA2215885235ATP2A1c.2013A= (p.Arg671=)
c.1638A= (p.Arg546=)
16g.28900829A>CCA494874437ATP2A1c.2013A>C (p.Arg671=)
c.1638A>C (p.Arg546=)
 dbSNP
16g.28900829A>GCA494874438ATP2A1c.2013A>G (p.Arg671=)
c.1638A>G (p.Arg546=)
16g.28900829A>TCA494874439ATP2A1c.2013A>T (p.Arg671=)
c.1638A>T (p.Arg546=)
 gnomAD v4
16g.28900830C>ACA395411413ATP2A1c.2014C>A (p.Arg672Ser)
c.1639C>A (p.Arg547Ser)
16g.28900830C=CA2215885244ATP2A1c.2014C= (p.Arg672=)
c.1639C= (p.Arg547=)
16g.28900830C>GCA395411414ATP2A1c.2014C>G (p.Arg672Gly)
c.1639C>G (p.Arg547Gly)
16g.28900830C>TCA7987148ATP2A1c.2014C>T (p.Arg672Cys)
c.1639C>T (p.Arg547Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900831G>ACA7987149ATP2A1c.2015G>A (p.Arg672His)
c.1640G>A (p.Arg547His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900831G>CCA395411415ATP2A1c.2015G>C (p.Arg672Pro)
c.1640G>C (p.Arg547Pro)
16g.28900831G=CA2215885247ATP2A1c.2015G= (p.Arg672=)
c.1640G= (p.Arg547=)
16g.28900831G>TCA395411416ATP2A1c.2015G>T (p.Arg672Leu)
c.1640G>T (p.Arg547Leu)
 dbSNP gnomAD v2
16g.28900832T>ACA494874440ATP2A1c.2016T>A (p.Arg672=)
c.1641T>A (p.Arg547=)
16g.28900832T>CCA494874441ATP2A1c.2016T>C (p.Arg672=)
c.1641T>C (p.Arg547=)
16g.28900832T>GCA494874442ATP2A1c.2016T>G (p.Arg672=)
c.1641T>G (p.Arg547=)
16g.28900833G>ACA395411417ATP2A1c.2017G>A (p.Ala673Thr)
c.1642G>A (p.Ala548Thr)
 gnomAD v4
16g.28900833G>CCA395411418ATP2A1c.2017G>C (p.Ala673Pro)
c.1642G>C (p.Ala548Pro)
16g.28900833G>TCA395411419ATP2A1c.2017G>T (p.Ala673Ser)
c.1642G>T (p.Ala548Ser)
16g.28900834C>ACA395411420ATP2A1c.2018C>A (p.Ala673Asp)
c.1643C>A (p.Ala548Asp)
 dbSNP gnomAD v4
16g.28900834C=CA2215885262ATP2A1c.2018C= (p.Ala673=)
c.1643C= (p.Ala548=)
16g.28900834C>GCA395411421ATP2A1c.2018C>G (p.Ala673Gly)
c.1643C>G (p.Ala548Gly)
16g.28900834C>TCA395411422ATP2A1c.2018C>T (p.Ala673Val)
c.1643C>T (p.Ala548Val)
16g.28900835C>ACA494874443ATP2A1c.2019C>A (p.Ala673=)
c.1644C>A (p.Ala548=)
16g.28900835C>GCA494874444ATP2A1c.2019C>G (p.Ala673=)
c.1644C>G (p.Ala548=)
16g.28900835C>TCA494874445ATP2A1c.2019C>T (p.Ala673=)
c.1644C>T (p.Ala548=)
16g.28900836T>ACA395411424ATP2A1c.2020T>A (p.Cys674Ser)
c.1645T>A (p.Cys549Ser)
16g.28900836T>CCA395411425ATP2A1c.2020T>C (p.Cys674Arg)
c.1645T>C (p.Cys549Arg)
 gnomAD v4
16g.28900836T>GCA395411423ATP2A1c.2020T>G (p.Cys674Gly)
c.1645T>G (p.Cys549Gly)
16g.28900837G>ACA279240442ATP2A1c.2021G>A (p.Cys674Tyr)
c.1646G>A (p.Cys549Tyr)
 ClinVar dbSNP gnomAD v4
16g.28900837G>CCA395411426ATP2A1c.2021G>C (p.Cys674Ser)
c.1646G>C (p.Cys549Ser)
16g.28900837G=CA2215885265ATP2A1c.2021G= (p.Cys674=)
c.1646G= (p.Cys549=)
16g.28900837G>TCA395411427ATP2A1c.2021G>T (p.Cys674Phe)
c.1646G>T (p.Cys549Phe)
16g.28900838C>ACA395411428ATP2A1c.2022C>A (p.Cys674Ter)
c.1647C>A (p.Cys549Ter)
16g.28900838C>GCA395411429ATP2A1c.2022C>G (p.Cys674Trp)
c.1647C>G (p.Cys549Trp)
16g.28900838C>TCA494874446ATP2A1c.2022C>T (p.Cys674=)
c.1647C>T (p.Cys549=)
16g.28900839T>ACA395411432ATP2A1c.2023T>A (p.Cys675Ser)
c.1648T>A (p.Cys550Ser)
16g.28900839T>CCA395411430ATP2A1c.2023T>C (p.Cys675Arg)
c.1648T>C (p.Cys550Arg)
 dbSNP gnomAD v2 gnomAD v4
16g.28900839T>GCA395411431ATP2A1c.2023T>G (p.Cys675Gly)
c.1648T>G (p.Cys550Gly)
16g.28900839T=CA2215885267ATP2A1c.2023T= (p.Cys675=)
c.1648T= (p.Cys550=)
16g.28900840G>ACA395411433ATP2A1c.2024G>A (p.Cys675Tyr)
c.1649G>A (p.Cys550Tyr)
 COSMIC COSMIC
16g.28900840G>CCA395411434ATP2A1c.2024G>C (p.Cys675Ser)
c.1649G>C (p.Cys550Ser)
 dbSNP gnomAD v3 gnomAD v4
16g.28900840G=CA2215885274ATP2A1c.2024G= (p.Cys675=)
c.1649G= (p.Cys550=)
16g.28900840G>TCA395411435ATP2A1c.2024G>T (p.Cys675Phe)
c.1649G>T (p.Cys550Phe)
16g.28900841C>ACA127436ATP2A1c.2025C>A (p.Cys675Ter)
c.1650C>A (p.Cys550Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.28900841C=CA2215885280ATP2A1c.2025C= (p.Cys675=)
c.1650C= (p.Cys550=)
16g.28900841C>GCA395411436ATP2A1c.2025C>G (p.Cys675Trp)
c.1650C>G (p.Cys550Trp)
16g.28900841C>TCA494874447ATP2A1c.2025C>T (p.Cys675=)
c.1650C>T (p.Cys550=)
16g.28900842T>ACA395411439ATP2A1c.2026T>A (p.Phe676Ile)
c.1651T>A (p.Phe551Ile)
16g.28900842T>CCA395411437ATP2A1c.2026T>C (p.Phe676Leu)
c.1651T>C (p.Phe551Leu)
16g.28900842T>GCA395411438ATP2A1c.2026T>G (p.Phe676Val)
c.1651T>G (p.Phe551Val)
16g.28900843T>ACA395411440ATP2A1c.2027T>A (p.Phe676Tyr)
c.1652T>A (p.Phe551Tyr)
16g.28900843T>CCA395411442ATP2A1c.2027T>C (p.Phe676Ser)
c.1652T>C (p.Phe551Ser)
16g.28900843T>GCA395411441ATP2A1c.2027T>G (p.Phe676Cys)
c.1652T>G (p.Phe551Cys)
16g.28900844C>ACA395411443ATP2A1c.2028C>A (p.Phe676Leu)
c.1653C>A (p.Phe551Leu)
16g.28900844C=CA2215885298ATP2A1c.2028C= (p.Phe676=)
c.1653C= (p.Phe551=)
16g.28900844C>GCA395411444ATP2A1c.2028C>G (p.Phe676Leu)
c.1653C>G (p.Phe551Leu)
16g.28900844C>TCA7987150ATP2A1c.2028C>T (p.Phe676=)
c.1653C>T (p.Phe551=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900845delCA2632540073ATP2A1c.2029del (p.Ala677ProfsTer24)
c.1654del (p.Ala552ProfsTer24)
 gnomAD v4
16g.28900845G>ACA7987151ATP2A1c.2029G>A (p.Ala677Thr)
c.1654G>A (p.Ala552Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900845G>CCA395411445ATP2A1c.2029G>C (p.Ala677Pro)
c.1654G>C (p.Ala552Pro)
16g.28900845G=CA2215885302ATP2A1c.2029G= (p.Ala677=)
c.1654G= (p.Ala552=)
16g.28900845G>TCA395411446ATP2A1c.2029G>T (p.Ala677Ser)
c.1654G>T (p.Ala552Ser)
 ClinVar dbSNP
16g.28900846C>ACA395411447ATP2A1c.2030C>A (p.Ala677Asp)
c.1655C>A (p.Ala552Asp)
16g.28900846C>GCA395411448ATP2A1c.2030C>G (p.Ala677Gly)
c.1655C>G (p.Ala552Gly)
16g.28900846C>TCA395411449ATP2A1c.2030C>T (p.Ala677Val)
c.1655C>T (p.Ala552Val)
 gnomAD v4
16g.28900847C>ACA494874450ATP2A1c.2031C>A (p.Ala677=)
c.1656C>A (p.Ala552=)
16g.28900847C>GCA494874449ATP2A1c.2031C>G (p.Ala677=)
c.1656C>G (p.Ala552=)
16g.28900847C>TCA494874448ATP2A1c.2031C>T (p.Ala677=)
c.1656C>T (p.Ala552=)
 gnomAD v4
16g.28900848C>ACA395411450ATP2A1c.2032C>A (p.Arg678Ser)
c.1657C>A (p.Arg553Ser)
16g.28900848C=CA2215885311ATP2A1c.2032C= (p.Arg678=)
c.1657C= (p.Arg553=)
16g.28900848C>GCA395411451ATP2A1c.2032C>G (p.Arg678Gly)
c.1657C>G (p.Arg553Gly)
16g.28900848C>TCA395411452ATP2A1c.2032C>T (p.Arg678Cys)
c.1657C>T (p.Arg553Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.28900849G>ACA7987152ATP2A1c.2033G>A (p.Arg678His)
c.1658G>A (p.Arg553His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900849G>CCA395411453ATP2A1c.2033G>C (p.Arg678Pro)
c.1658G>C (p.Arg553Pro)
16g.28900849G=CA2215885315ATP2A1c.2033G= (p.Arg678=)
c.1658G= (p.Arg553=)
16g.28900849G>TCA395411454ATP2A1c.2033G>T (p.Arg678Leu)
c.1658G>T (p.Arg553Leu)
 dbSNP gnomAD v2 gnomAD v4
16g.28900850T>ACA494874453ATP2A1c.2034T>A (p.Arg678=)
c.1659T>A (p.Arg553=)
16g.28900850T>CCA494874452ATP2A1c.2034T>C (p.Arg678=)
c.1659T>C (p.Arg553=)
 dbSNP gnomAD v4
16g.28900850T>GCA494874451ATP2A1c.2034T>G (p.Arg678=)
c.1659T>G (p.Arg553=)
16g.28900850T=CA2215885321ATP2A1c.2034T= (p.Arg678=)
c.1659T= (p.Arg553=)
16g.28900851G>ACA395411455ATP2A1c.2035G>A (p.Val679Met)
c.1660G>A (p.Val554Met)
 gnomAD v4
16g.28900851G>CCA395411456ATP2A1c.2035G>C (p.Val679Leu)
c.1660G>C (p.Val554Leu)
16g.28900851G>TCA395411457ATP2A1c.2035G>T (p.Val679Leu)
c.1660G>T (p.Val554Leu)
16g.28900852T>ACA395411458ATP2A1c.2036T>A (p.Val679Glu)
c.1661T>A (p.Val554Glu)
16g.28900852T>CCA7987153ATP2A1c.2036T>C (p.Val679Ala)
c.1661T>C (p.Val554Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900852T>GCA395411459ATP2A1c.2036T>G (p.Val679Gly)
c.1661T>G (p.Val554Gly)
16g.28900852T=CA2215885325ATP2A1c.2036T= (p.Val679=)
c.1661T= (p.Val554=)
16g.28900853G>ACA494874454ATP2A1c.2037G>A (p.Val679=)
c.1662G>A (p.Val554=)
 COSMIC COSMIC
16g.28900853G>CCA494874456ATP2A1c.2037G>C (p.Val679=)
c.1662G>C (p.Val554=)
16g.28900853G>TCA494874455ATP2A1c.2037G>T (p.Val679=)
c.1662G>T (p.Val554=)
16g.28900854G>ACA395411460ATP2A1c.2038G>A (p.Glu680Lys)
c.1663G>A (p.Glu555Lys)
16g.28900854G>CCA395411461ATP2A1c.2038G>C (p.Glu680Gln)
c.1663G>C (p.Glu555Gln)
16g.28900854G>TCA395411462ATP2A1c.2038G>T (p.Glu680Ter)
c.1663G>T (p.Glu555Ter)
16g.28900855A>CCA395411463ATP2A1c.2039A>C (p.Glu680Ala)
c.1664A>C (p.Glu555Ala)
16g.28900855A>GCA395411464ATP2A1c.2039A>G (p.Glu680Gly)
c.1664A>G (p.Glu555Gly)
16g.28900855A>TCA395411465ATP2A1c.2039A>T (p.Glu680Val)
c.1664A>T (p.Glu555Val)
 COSMIC
16g.28900856G>ACA494874457ATP2A1c.2040G>A (p.Glu680=)
c.1665G>A (p.Glu555=)
16g.28900856G>CCA395411466ATP2A1c.2040G>C (p.Glu680Asp)
c.1665G>C (p.Glu555Asp)
16g.28900856G=CA2215885331ATP2A1c.2040G= (p.Glu680=)
c.1665G= (p.Glu555=)
16g.28900856G>TCA7987154ATP2A1c.2040G>T (p.Glu680Asp)
c.1665G>T (p.Glu555Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched