Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41977940G>ACA406044792ATP1A3c.1978C>T (p.Pro660Ser)
c.1939C>T (p.Pro647Ser)
c.1972C>T (p.Pro658Ser)
c.1849C>T (p.Pro617Ser)
19g.41977940G>CCA406044794ATP1A3c.1978C>G (p.Pro660Ala)
c.1939C>G (p.Pro647Ala)
c.1972C>G (p.Pro658Ala)
c.1849C>G (p.Pro617Ala)
19g.41977940G>TCA406044796ATP1A3c.1978C>A (p.Pro660Thr)
c.1939C>A (p.Pro647Thr)
c.1972C>A (p.Pro658Thr)
c.1849C>A (p.Pro617Thr)
19g.41977941G>ACA507586293ATP1A3c.1977C>T (p.Asn659=)
c.1938C>T (p.Asn646=)
c.1971C>T (p.Asn657=)
c.1848C>T (p.Asn616=)
dbSNP gnomAD v2 gnomAD v4
19g.41977941G>CCA406044798ATP1A3c.1977C>G (p.Asn659Lys)
c.1938C>G (p.Asn646Lys)
c.1971C>G (p.Asn657Lys)
c.1848C>G (p.Asn616Lys)
COSMIC
19g.41977941G=CA2336724819ATP1A3c.1977C= (p.Asn659=)
c.1938C= (p.Asn646=)
c.1971C= (p.Asn657=)
c.1848C= (p.Asn616=)
19g.41977941G>TCA406044800ATP1A3c.1977C>A (p.Asn659Lys)
c.1938C>A (p.Asn646Lys)
c.1971C>A (p.Asn657Lys)
c.1848C>A (p.Asn616Lys)
dbSNP
19g.41977942T>ACA406044802ATP1A3c.1976A>T (p.Asn659Ile)
c.1937A>T (p.Asn646Ile)
c.1970A>T (p.Asn657Ile)
c.1847A>T (p.Asn616Ile)
19g.41977942T>CCA406044805ATP1A3c.1976A>G (p.Asn659Ser)
c.1937A>G (p.Asn646Ser)
c.1970A>G (p.Asn657Ser)
c.1847A>G (p.Asn616Ser)
19g.41977942T>GCA406044803ATP1A3c.1976A>C (p.Asn659Thr)
c.1937A>C (p.Asn646Thr)
c.1970A>C (p.Asn657Thr)
c.1847A>C (p.Asn616Thr)
19g.41977943T>ACA406044807ATP1A3c.1975A>T (p.Asn659Tyr)
c.1936A>T (p.Asn646Tyr)
c.1969A>T (p.Asn657Tyr)
c.1846A>T (p.Asn616Tyr)
19g.41977943T>CCA406044809ATP1A3c.1975A>G (p.Asn659Asp)
c.1936A>G (p.Asn646Asp)
c.1969A>G (p.Asn657Asp)
c.1846A>G (p.Asn616Asp)
19g.41977943T>GCA406044811ATP1A3c.1975A>C (p.Asn659His)
c.1936A>C (p.Asn646His)
c.1969A>C (p.Asn657His)
c.1846A>C (p.Asn616His)
19g.41977944A>CCA507586304ATP1A3c.1974T>G (p.Val658=)
c.1935T>G (p.Val645=)
c.1968T>G (p.Val656=)
c.1845T>G (p.Val615=)
19g.41977944A>GCA507586306ATP1A3c.1974T>C (p.Val658=)
c.1935T>C (p.Val645=)
c.1968T>C (p.Val656=)
c.1845T>C (p.Val615=)
19g.41977944A>TCA507586308ATP1A3c.1974T>A (p.Val658=)
c.1935T>A (p.Val645=)
c.1968T>A (p.Val656=)
c.1845T>A (p.Val615=)
19g.41977945A>CCA406044813ATP1A3c.1973T>G (p.Val658Gly)
c.1934T>G (p.Val645Gly)
c.1967T>G (p.Val656Gly)
c.1844T>G (p.Val615Gly)
19g.41977945A>GCA406044815ATP1A3c.1973T>C (p.Val658Ala)
c.1934T>C (p.Val645Ala)
c.1967T>C (p.Val656Ala)
c.1844T>C (p.Val615Ala)
COSMIC
19g.41977945A>TCA406044817ATP1A3c.1973T>A (p.Val658Asp)
c.1934T>A (p.Val645Asp)
c.1967T>A (p.Val656Asp)
c.1844T>A (p.Val615Asp)
19g.41977946C>ACA406044819ATP1A3c.1972G>T (p.Val658Phe)
c.1933G>T (p.Val645Phe)
c.1966G>T (p.Val656Phe)
c.1843G>T (p.Val615Phe)
19g.41977946C>GCA406044821ATP1A3c.1972G>C (p.Val658Leu)
c.1933G>C (p.Val645Leu)
c.1966G>C (p.Val656Leu)
c.1843G>C (p.Val615Leu)
19g.41977946C>TCA406044823ATP1A3c.1972G>A (p.Val658Ile)
c.1933G>A (p.Val645Ile)
c.1966G>A (p.Val656Ile)
c.1843G>A (p.Val615Ile)
19g.41977947C>ACA406044825ATP1A3c.1971G>T (p.Gln657His)
c.1932G>T (p.Gln644His)
c.1965G>T (p.Gln655His)
c.1842G>T (p.Gln614His)
19g.41977947C=CA2336724820ATP1A3c.1971G= (p.Gln657=)
c.1932G= (p.Gln644=)
c.1965G= (p.Gln655=)
c.1842G= (p.Gln614=)
19g.41977947C>GCA406044826ATP1A3c.1971G>C (p.Gln657His)
c.1932G>C (p.Gln644His)
c.1965G>C (p.Gln655His)
c.1842G>C (p.Gln614His)
ClinVar
19g.41977947C>TCA507586320ATP1A3c.1971G>A (p.Gln657=)
c.1932G>A (p.Gln644=)
c.1965G>A (p.Gln655=)
c.1842G>A (p.Gln614=)
ClinVar dbSNP
19g.41977948T>ACA16616279ATP1A3c.1970A>T (p.Gln657Leu)
c.1931A>T (p.Gln644Leu)
c.1964A>T (p.Gln655Leu)
c.1841A>T (p.Gln614Leu)
ClinVar dbSNP
19g.41977948T>CCA406044830ATP1A3c.1970A>G (p.Gln657Arg)
c.1931A>G (p.Gln644Arg)
c.1964A>G (p.Gln655Arg)
c.1841A>G (p.Gln614Arg)
19g.41977948T>GCA406044829ATP1A3c.1970A>C (p.Gln657Pro)
c.1931A>C (p.Gln644Pro)
c.1964A>C (p.Gln655Pro)
c.1841A>C (p.Gln614Pro)
19g.41977948T=CA2336724821ATP1A3c.1970A= (p.Gln657=)
c.1931A= (p.Gln644=)
c.1964A= (p.Gln655=)
c.1841A= (p.Gln614=)
19g.41977949G>ACA406044833ATP1A3c.1969C>T (p.Gln657Ter)
c.1930C>T (p.Gln644Ter)
c.1963C>T (p.Gln655Ter)
c.1840C>T (p.Gln614Ter)
ClinVar dbSNP
19g.41977949G>CCA406044835ATP1A3c.1969C>G (p.Gln657Glu)
c.1930C>G (p.Gln644Glu)
c.1963C>G (p.Gln655Glu)
c.1840C>G (p.Gln614Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41977949G=CA2336724822ATP1A3c.1969C= (p.Gln657=)
c.1930C= (p.Gln644=)
c.1963C= (p.Gln655=)
c.1840C= (p.Gln614=)
19g.41977949G>TCA406044837ATP1A3c.1969C>A (p.Gln657Lys)
c.1930C>A (p.Gln644Lys)
c.1963C>A (p.Gln655Lys)
c.1840C>A (p.Gln614Lys)
19g.41977950G>ACA507586329ATP1A3c.1968C>T (p.Ser656=)
c.1929C>T (p.Ser643=)
c.1962C>T (p.Ser654=)
c.1839C>T (p.Ser613=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41977950G>CCA406044839ATP1A3c.1968C>G (p.Ser656Arg)
c.1929C>G (p.Ser643Arg)
c.1962C>G (p.Ser654Arg)
c.1839C>G (p.Ser613Arg)
19g.41977950G=CA2336724823ATP1A3c.1968C= (p.Ser656=)
c.1929C= (p.Ser643=)
c.1962C= (p.Ser654=)
c.1839C= (p.Ser613=)
19g.41977950G>TCA406044841ATP1A3c.1968C>A (p.Ser656Arg)
c.1929C>A (p.Ser643Arg)
c.1962C>A (p.Ser654Arg)
c.1839C>A (p.Ser613Arg)
19g.41977951C>ACA406044846ATP1A3c.1967G>T (p.Ser656Ile)
c.1928G>T (p.Ser643Ile)
c.1961G>T (p.Ser654Ile)
c.1838G>T (p.Ser613Ile)
19g.41977951C>GCA406044845ATP1A3c.1967G>C (p.Ser656Thr)
c.1928G>C (p.Ser643Thr)
c.1961G>C (p.Ser654Thr)
c.1838G>C (p.Ser613Thr)
ClinVar
19g.41977951C>TCA406044843ATP1A3c.1967G>A (p.Ser656Asn)
c.1928G>A (p.Ser643Asn)
c.1961G>A (p.Ser654Asn)
c.1838G>A (p.Ser613Asn)
ClinVar dbSNP
19g.41977952T>ACA406044849ATP1A3c.1966A>T (p.Ser656Cys)
c.1927A>T (p.Ser643Cys)
c.1960A>T (p.Ser654Cys)
c.1837A>T (p.Ser613Cys)
19g.41977952T>CCA406044850ATP1A3c.1966A>G (p.Ser656Gly)
c.1927A>G (p.Ser643Gly)
c.1960A>G (p.Ser654Gly)
c.1837A>G (p.Ser613Gly)
19g.41977952T>GCA406044851ATP1A3c.1966A>C (p.Ser656Arg)
c.1927A>C (p.Ser643Arg)
c.1960A>C (p.Ser654Arg)
c.1837A>C (p.Ser613Arg)
19g.41977953G>ACA507586351ATP1A3c.1965C>T (p.Val655=)
c.1926C>T (p.Val642=)
c.1959C>T (p.Val653=)
c.1836C>T (p.Val612=)
gnomAD v4
19g.41977953G>CCA507586355ATP1A3c.1965C>G (p.Val655=)
c.1926C>G (p.Val642=)
c.1959C>G (p.Val653=)
c.1836C>G (p.Val612=)
19g.41977953G>TCA507586353ATP1A3c.1965C>A (p.Val655=)
c.1926C>A (p.Val642=)
c.1959C>A (p.Val653=)
c.1836C>A (p.Val612=)
19g.41977954A>CCA406044854ATP1A3c.1964T>G (p.Val655Gly)
c.1925T>G (p.Val642Gly)
c.1958T>G (p.Val653Gly)
c.1835T>G (p.Val612Gly)
19g.41977954A>GCA406044855ATP1A3c.1964T>C (p.Val655Ala)
c.1925T>C (p.Val642Ala)
c.1958T>C (p.Val653Ala)
c.1835T>C (p.Val612Ala)
19g.41977954A>TCA406044857ATP1A3c.1964T>A (p.Val655Asp)
c.1925T>A (p.Val642Asp)
c.1958T>A (p.Val653Asp)
c.1835T>A (p.Val612Asp)
gnomAD v4
19g.41977955C>ACA406044862ATP1A3c.1963G>T (p.Val655Phe)
c.1924G>T (p.Val642Phe)
c.1957G>T (p.Val653Phe)
c.1834G>T (p.Val612Phe)
dbSNP
19g.41977955C=CA2336724824ATP1A3c.1963G= (p.Val655=)
c.1924G= (p.Val642=)
c.1957G= (p.Val653=)
c.1834G= (p.Val612=)
19g.41977955C>GCA406044860ATP1A3c.1963G>C (p.Val655Leu)
c.1924G>C (p.Val642Leu)
c.1957G>C (p.Val653Leu)
c.1834G>C (p.Val612Leu)
dbSNP gnomAD v2 gnomAD v4
19g.41977955C>TCA9467537ATP1A3c.1963G>A (p.Val655Ile)
c.1924G>A (p.Val642Ile)
c.1957G>A (p.Val653Ile)
c.1834G>A (p.Val612Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41977956G>ACA9467538ATP1A3c.1962C>T (p.Pro654=)
c.1923C>T (p.Pro641=)
c.1956C>T (p.Pro652=)
c.1833C>T (p.Pro611=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41977956G>CCA9467539ATP1A3c.1962C>G (p.Pro654=)
c.1923C>G (p.Pro641=)
c.1956C>G (p.Pro652=)
c.1833C>G (p.Pro611=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41977956G=CA2336724825ATP1A3c.1962C= (p.Pro654=)
c.1923C= (p.Pro641=)
c.1956C= (p.Pro652=)
c.1833C= (p.Pro611=)
19g.41977956G>TCA507586366ATP1A3c.1962C>A (p.Pro654=)
c.1923C>A (p.Pro641=)
c.1956C>A (p.Pro652=)
c.1833C>A (p.Pro611=)
19g.41977957G>ACA406044866ATP1A3c.1961C>T (p.Pro654Leu)
c.1922C>T (p.Pro641Leu)
c.1955C>T (p.Pro652Leu)
c.1832C>T (p.Pro611Leu)
19g.41977957G>CCA406044867ATP1A3c.1961C>G (p.Pro654Arg)
c.1922C>G (p.Pro641Arg)
c.1955C>G (p.Pro652Arg)
c.1832C>G (p.Pro611Arg)
19g.41977957G>TCA406044869ATP1A3c.1961C>A (p.Pro654His)
c.1922C>A (p.Pro641His)
c.1955C>A (p.Pro652His)
c.1832C>A (p.Pro611His)
19g.41977958G>ACA406044871ATP1A3c.1960C>T (p.Pro654Ser)
c.1921C>T (p.Pro641Ser)
c.1954C>T (p.Pro652Ser)
c.1831C>T (p.Pro611Ser)
19g.41977958G>CCA406044873ATP1A3c.1960C>G (p.Pro654Ala)
c.1921C>G (p.Pro641Ala)
c.1954C>G (p.Pro652Ala)
c.1831C>G (p.Pro611Ala)
19g.41977958G>TCA406044875ATP1A3c.1960C>A (p.Pro654Thr)
c.1921C>A (p.Pro641Thr)
c.1954C>A (p.Pro652Thr)
c.1831C>A (p.Pro611Thr)
19g.41977959A>CCA406044877ATP1A3c.1959T>G (p.Ile653Met)
c.1920T>G (p.Ile640Met)
c.1953T>G (p.Ile651Met)
c.1830T>G (p.Ile610Met)
19g.41977959A>GCA507586378ATP1A3c.1959T>C (p.Ile653=)
c.1920T>C (p.Ile640=)
c.1953T>C (p.Ile651=)
c.1830T>C (p.Ile610=)
19g.41977959A>TCA507586380ATP1A3c.1959T>A (p.Ile653=)
c.1920T>A (p.Ile640=)
c.1953T>A (p.Ile651=)
c.1830T>A (p.Ile610=)
19g.41977960A>CCA406044880ATP1A3c.1958T>G (p.Ile653Ser)
c.1919T>G (p.Ile640Ser)
c.1952T>G (p.Ile651Ser)
c.1829T>G (p.Ile610Ser)
19g.41977960A>GCA406044881ATP1A3c.1958T>C (p.Ile653Thr)
c.1919T>C (p.Ile640Thr)
c.1952T>C (p.Ile651Thr)
c.1829T>C (p.Ile610Thr)
gnomAD v4
19g.41977960A>TCA406044883ATP1A3c.1958T>A (p.Ile653Asn)
c.1919T>A (p.Ile640Asn)
c.1952T>A (p.Ile651Asn)
c.1829T>A (p.Ile610Asn)
19g.41977961T>ACA406044885ATP1A3c.1957A>T (p.Ile653Phe)
c.1918A>T (p.Ile640Phe)
c.1951A>T (p.Ile651Phe)
c.1828A>T (p.Ile610Phe)
19g.41977961T>CCA406044889ATP1A3c.1957A>G (p.Ile653Val)
c.1918A>G (p.Ile640Val)
c.1951A>G (p.Ile651Val)
c.1828A>G (p.Ile610Val)
dbSNP gnomAD v3 gnomAD v4
19g.41977961T>GCA406044887ATP1A3c.1957A>C (p.Ile653Leu)
c.1918A>C (p.Ile640Leu)
c.1951A>C (p.Ile651Leu)
c.1828A>C (p.Ile610Leu)
19g.41977961T=CA2336724826ATP1A3c.1957A= (p.Ile653=)
c.1918A= (p.Ile640=)
c.1951A= (p.Ile651=)
c.1828A= (p.Ile610=)
19g.41977962G>ACA507586396ATP1A3c.1956C>T (p.Asn652=)
c.1917C>T (p.Asn639=)
c.1950C>T (p.Asn650=)
c.1827C>T (p.Asn609=)
ClinVar dbSNP
19g.41977962G>CCA406044891ATP1A3c.1956C>G (p.Asn652Lys)
c.1917C>G (p.Asn639Lys)
c.1950C>G (p.Asn650Lys)
c.1827C>G (p.Asn609Lys)
19g.41977962G>TCA406044892ATP1A3c.1956C>A (p.Asn652Lys)
c.1917C>A (p.Asn639Lys)
c.1950C>A (p.Asn650Lys)
c.1827C>A (p.Asn609Lys)
19g.41977963T>ACA406044895ATP1A3c.1955A>T (p.Asn652Ile)
c.1916A>T (p.Asn639Ile)
c.1949A>T (p.Asn650Ile)
c.1826A>T (p.Asn609Ile)
19g.41977963T>CCA406044897ATP1A3c.1955A>G (p.Asn652Ser)
c.1916A>G (p.Asn639Ser)
c.1949A>G (p.Asn650Ser)
c.1826A>G (p.Asn609Ser)
19g.41977963T>GCA406044899ATP1A3c.1955A>C (p.Asn652Thr)
c.1916A>C (p.Asn639Thr)
c.1949A>C (p.Asn650Thr)
c.1826A>C (p.Asn609Thr)
19g.41977964T>ACA406044901ATP1A3c.1954A>T (p.Asn652Tyr)
c.1915A>T (p.Asn639Tyr)
c.1948A>T (p.Asn650Tyr)
c.1825A>T (p.Asn609Tyr)
19g.41977964T>CCA9467540ATP1A3c.1954A>G (p.Asn652Asp)
c.1915A>G (p.Asn639Asp)
c.1948A>G (p.Asn650Asp)
c.1825A>G (p.Asn609Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.41977964T>GCA406044904ATP1A3c.1954A>C (p.Asn652His)
c.1915A>C (p.Asn639His)
c.1948A>C (p.Asn650His)
c.1825A>C (p.Asn609His)
19g.41977964T=CA2336724827ATP1A3c.1954A= (p.Asn652=)
c.1915A= (p.Asn639=)
c.1948A= (p.Asn650=)
c.1825A= (p.Asn609=)
19g.41977965G>ACA507586408ATP1A3c.1953C>T (p.Leu651=)
c.1914C>T (p.Leu638=)
c.1947C>T (p.Leu649=)
c.1824C>T (p.Leu608=)
19g.41977965G>CCA507586411ATP1A3c.1953C>G (p.Leu651=)
c.1914C>G (p.Leu638=)
c.1947C>G (p.Leu649=)
c.1824C>G (p.Leu608=)
19g.41977965G>TCA507586414ATP1A3c.1953C>A (p.Leu651=)
c.1914C>A (p.Leu638=)
c.1947C>A (p.Leu649=)
c.1824C>A (p.Leu608=)
19g.41977966A>CCA406044906ATP1A3c.1952T>G (p.Leu651Arg)
c.1913T>G (p.Leu638Arg)
c.1946T>G (p.Leu649Arg)
c.1823T>G (p.Leu608Arg)
19g.41977966A>GCA406044908ATP1A3c.1952T>C (p.Leu651Pro)
c.1913T>C (p.Leu638Pro)
c.1946T>C (p.Leu649Pro)
c.1823T>C (p.Leu608Pro)
19g.41977966A>TCA406044910ATP1A3c.1952T>A (p.Leu651His)
c.1913T>A (p.Leu638His)
c.1946T>A (p.Leu649His)
c.1823T>A (p.Leu608His)
19g.41977967G>ACA406044916ATP1A3c.1951C>T (p.Leu651Phe)
c.1912C>T (p.Leu638Phe)
c.1945C>T (p.Leu649Phe)
c.1822C>T (p.Leu608Phe)
dbSNP gnomAD v2
19g.41977967G>CCA406044914ATP1A3c.1951C>G (p.Leu651Val)
c.1912C>G (p.Leu638Val)
c.1945C>G (p.Leu649Val)
c.1822C>G (p.Leu608Val)
19g.41977967G=CA2336724828ATP1A3c.1951C= (p.Leu651=)
c.1912C= (p.Leu638=)
c.1945C= (p.Leu649=)
c.1822C= (p.Leu608=)
19g.41977967G>TCA406044912ATP1A3c.1951C>A (p.Leu651Ile)
c.1912C>A (p.Leu638Ile)
c.1945C>A (p.Leu649Ile)
c.1822C>A (p.Leu608Ile)
19g.41977968C>ACA507586424ATP1A3c.1950G>T (p.Arg650=)
c.1911G>T (p.Arg637=)
c.1944G>T (p.Arg648=)
c.1821G>T (p.Arg607=)
gnomAD v4
19g.41977968C=CA2336724829ATP1A3c.1950G= (p.Arg650=)
c.1911G= (p.Arg637=)
c.1944G= (p.Arg648=)
c.1821G= (p.Arg607=)
19g.41977968C>GCA507586426ATP1A3c.1950G>C (p.Arg650=)
c.1911G>C (p.Arg637=)
c.1944G>C (p.Arg648=)
c.1821G>C (p.Arg607=)
19g.41977968C>TCA507586429ATP1A3c.1950G>A (p.Arg650=)
c.1911G>A (p.Arg637=)
c.1944G>A (p.Arg648=)
c.1821G>A (p.Arg607=)
dbSNP gnomAD v4 COSMIC
19g.41977969C>ACA406044918ATP1A3c.1949G>T (p.Arg650Leu)
c.1910G>T (p.Arg637Leu)
c.1943G>T (p.Arg648Leu)
c.1820G>T (p.Arg607Leu)
19g.41977969C=CA2336724830ATP1A3c.1949G= (p.Arg650=)
c.1910G= (p.Arg637=)
c.1943G= (p.Arg648=)
c.1820G= (p.Arg607=)
19g.41977969C>GCA406044920ATP1A3c.1949G>C (p.Arg650Pro)
c.1910G>C (p.Arg637Pro)
c.1943G>C (p.Arg648Pro)
c.1820G>C (p.Arg607Pro)
19g.41977969C>TCA406044922ATP1A3c.1949G>A (p.Arg650Gln)
c.1910G>A (p.Arg637Gln)
c.1943G>A (p.Arg648Gln)
c.1820G>A (p.Arg607Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41977970G>ACA406044924ATP1A3c.1948C>T (p.Arg650Trp)
c.1909C>T (p.Arg637Trp)
c.1942C>T (p.Arg648Trp)
c.1819C>T (p.Arg607Trp)
dbSNP gnomAD v2 gnomAD v4
19g.41977970G>CCA406044926ATP1A3c.1948C>G (p.Arg650Gly)
c.1909C>G (p.Arg637Gly)
c.1942C>G (p.Arg648Gly)
c.1819C>G (p.Arg607Gly)
19g.41977970G=CA2336724831ATP1A3c.1948C= (p.Arg650=)
c.1909C= (p.Arg637=)
c.1942C= (p.Arg648=)
c.1819C= (p.Arg607=)
19g.41977970G>TCA507586437ATP1A3c.1948C>A (p.Arg650=)
c.1909C>A (p.Arg637=)
c.1942C>A (p.Arg648=)
c.1819C>A (p.Arg607=)
19g.41977971G>ACA507586440ATP1A3c.1947C>T (p.Ala649=)
c.1908C>T (p.Ala636=)
c.1941C>T (p.Ala647=)
c.1818C>T (p.Ala606=)
19g.41977971G>CCA507586442ATP1A3c.1947C>G (p.Ala649=)
c.1908C>G (p.Ala636=)
c.1941C>G (p.Ala647=)
c.1818C>G (p.Ala606=)
19g.41977971G>TCA507586445ATP1A3c.1947C>A (p.Ala649=)
c.1908C>A (p.Ala636=)
c.1941C>A (p.Ala647=)
c.1818C>A (p.Ala606=)
19g.41977972G>ACA406044928ATP1A3c.1946C>T (p.Ala649Val)
c.1907C>T (p.Ala636Val)
c.1940C>T (p.Ala647Val)
c.1817C>T (p.Ala606Val)
19g.41977972G>CCA406044930ATP1A3c.1946C>G (p.Ala649Gly)
c.1907C>G (p.Ala636Gly)
c.1940C>G (p.Ala647Gly)
c.1817C>G (p.Ala606Gly)
19g.41977972G>TCA406044932ATP1A3c.1946C>A (p.Ala649Asp)
c.1907C>A (p.Ala636Asp)
c.1940C>A (p.Ala647Asp)
c.1817C>A (p.Ala606Asp)
19g.41977973C>ACA406044933ATP1A3c.1945G>T (p.Ala649Ser)
c.1906G>T (p.Ala636Ser)
c.1939G>T (p.Ala647Ser)
c.1816G>T (p.Ala606Ser)
ClinVar dbSNP
19g.41977973C=CA2336724832ATP1A3c.1945G= (p.Ala649=)
c.1906G= (p.Ala636=)
c.1939G= (p.Ala647=)
c.1816G= (p.Ala606=)
19g.41977973C>GCA406044934ATP1A3c.1945G>C (p.Ala649Pro)
c.1906G>C (p.Ala636Pro)
c.1939G>C (p.Ala647Pro)
c.1816G>C (p.Ala606Pro)
19g.41977973C>TCA9467541ATP1A3c.1945G>A (p.Ala649Thr)
c.1906G>A (p.Ala636Thr)
c.1939G>A (p.Ala647Thr)
c.1816G>A (p.Ala606Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41977974G>ACA9467542ATP1A3c.1944C>T (p.Ala648=)
c.1905C>T (p.Ala635=)
c.1938C>T (p.Ala646=)
c.1815C>T (p.Ala605=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41977974G>CCA507586455ATP1A3c.1944C>G (p.Ala648=)
c.1905C>G (p.Ala635=)
c.1938C>G (p.Ala646=)
c.1815C>G (p.Ala605=)
19g.41977974G=CA2336724833ATP1A3c.1944C= (p.Ala648=)
c.1905C= (p.Ala635=)
c.1938C= (p.Ala646=)
c.1815C= (p.Ala605=)
19g.41977974G>TCA507586456ATP1A3c.1944C>A (p.Ala648=)
c.1905C>A (p.Ala635=)
c.1938C>A (p.Ala646=)
c.1815C>A (p.Ala605=)
19g.41977975G>ACA406044941ATP1A3c.1943C>T (p.Ala648Val)
c.1904C>T (p.Ala635Val)
c.1937C>T (p.Ala646Val)
c.1814C>T (p.Ala605Val)
19g.41977975G>CCA406044939ATP1A3c.1943C>G (p.Ala648Gly)
c.1904C>G (p.Ala635Gly)
c.1937C>G (p.Ala646Gly)
c.1814C>G (p.Ala605Gly)
19g.41977975G>TCA406044937ATP1A3c.1943C>A (p.Ala648Asp)
c.1904C>A (p.Ala635Asp)
c.1937C>A (p.Ala646Asp)
c.1814C>A (p.Ala605Asp)
19g.41977976C>ACA406044943ATP1A3c.1942G>T (p.Ala648Ser)
c.1903G>T (p.Ala635Ser)
c.1936G>T (p.Ala646Ser)
c.1813G>T (p.Ala605Ser)
dbSNP gnomAD v3 gnomAD v4
19g.41977976C=CA2336724834ATP1A3c.1942G= (p.Ala648=)
c.1903G= (p.Ala635=)
c.1936G= (p.Ala646=)
c.1813G= (p.Ala605=)
19g.41977976C>GCA406044946ATP1A3c.1942G>C (p.Ala648Pro)
c.1903G>C (p.Ala635Pro)
c.1936G>C (p.Ala646Pro)
c.1813G>C (p.Ala605Pro)
19g.41977976C>TCA9467543ATP1A3c.1942G>A (p.Ala648Thr)
c.1903G>A (p.Ala635Thr)
c.1936G>A (p.Ala646Thr)
c.1813G>A (p.Ala605Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41977977G>ACA507586460ATP1A3c.1941C>T (p.Ile647=)
c.1902C>T (p.Ile634=)
c.1935C>T (p.Ile645=)
c.1812C>T (p.Ile604=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41977977G>CCA406044948ATP1A3c.1941C>G (p.Ile647Met)
c.1902C>G (p.Ile634Met)
c.1935C>G (p.Ile645Met)
c.1812C>G (p.Ile604Met)
19g.41977977G=CA2336724835ATP1A3c.1941C= (p.Ile647=)
c.1902C= (p.Ile634=)
c.1935C= (p.Ile645=)
c.1812C= (p.Ile604=)
19g.41977977G>TCA507586463ATP1A3c.1941C>A (p.Ile647=)
c.1902C>A (p.Ile634=)
c.1935C>A (p.Ile645=)
c.1812C>A (p.Ile604=)
19g.41977978A>CCA406044952ATP1A3c.1940T>G (p.Ile647Ser)
c.1901T>G (p.Ile634Ser)
c.1934T>G (p.Ile645Ser)
c.1811T>G (p.Ile604Ser)
19g.41977978A>GCA406044951ATP1A3c.1940T>C (p.Ile647Thr)
c.1901T>C (p.Ile634Thr)
c.1934T>C (p.Ile645Thr)
c.1811T>C (p.Ile604Thr)
19g.41977978A>TCA406044954ATP1A3c.1940T>A (p.Ile647Asn)
c.1901T>A (p.Ile634Asn)
c.1934T>A (p.Ile645Asn)
c.1811T>A (p.Ile604Asn)
19g.41977979T>ACA406044957ATP1A3c.1939A>T (p.Ile647Phe)
c.1900A>T (p.Ile634Phe)
c.1933A>T (p.Ile645Phe)
c.1810A>T (p.Ile604Phe)
19g.41977979T>CCA406044958ATP1A3c.1939A>G (p.Ile647Val)
c.1900A>G (p.Ile634Val)
c.1933A>G (p.Ile645Val)
c.1810A>G (p.Ile604Val)
dbSNP gnomAD v2
19g.41977979T>GCA406044960ATP1A3c.1939A>C (p.Ile647Leu)
c.1900A>C (p.Ile634Leu)
c.1933A>C (p.Ile645Leu)
c.1810A>C (p.Ile604Leu)
19g.41977979T=CA2336724836ATP1A3c.1939A= (p.Ile647=)
c.1900A= (p.Ile634=)
c.1933A= (p.Ile645=)
c.1810A= (p.Ile604=)
19g.41977980G>ACA507586472ATP1A3c.1938C>T (p.Asp646=)
c.1899C>T (p.Asp633=)
c.1932C>T (p.Asp644=)
c.1809C>T (p.Asp603=)
gnomAD v4
19g.41977980G>CCA406044963ATP1A3c.1938C>G (p.Asp646Glu)
c.1899C>G (p.Asp633Glu)
c.1932C>G (p.Asp644Glu)
c.1809C>G (p.Asp603Glu)
19g.41977980G=CA2336724837ATP1A3c.1938C= (p.Asp646=)
c.1899C= (p.Asp633=)
c.1932C= (p.Asp644=)
c.1809C= (p.Asp603=)
19g.41977980G>TCA406044964ATP1A3c.1938C>A (p.Asp646Glu)
c.1899C>A (p.Asp633Glu)
c.1932C>A (p.Asp644Glu)
c.1809C>A (p.Asp603Glu)
ClinVar dbSNP
19g.41977981T>ACA406044967ATP1A3c.1937A>T (p.Asp646Val)
c.1898A>T (p.Asp633Val)
c.1931A>T (p.Asp644Val)
c.1808A>T (p.Asp603Val)
19g.41977981T>CCA406044969ATP1A3c.1937A>G (p.Asp646Gly)
c.1898A>G (p.Asp633Gly)
c.1931A>G (p.Asp644Gly)
c.1808A>G (p.Asp603Gly)
19g.41977981T>GCA406044970ATP1A3c.1937A>C (p.Asp646Ala)
c.1898A>C (p.Asp633Ala)
c.1931A>C (p.Asp644Ala)
c.1808A>C (p.Asp603Ala)
19g.41977982C>ACA406044971ATP1A3c.1936G>T (p.Asp646Tyr)
c.1897G>T (p.Asp633Tyr)
c.1930G>T (p.Asp644Tyr)
c.1807G>T (p.Asp603Tyr)
19g.41977982C>GCA406044972ATP1A3c.1936G>C (p.Asp646His)
c.1897G>C (p.Asp633His)
c.1930G>C (p.Asp644His)
c.1807G>C (p.Asp603His)
19g.41977982C>TCA406044973ATP1A3c.1936G>A (p.Asp646Asn)
c.1897G>A (p.Asp633Asn)
c.1930G>A (p.Asp644Asn)
c.1807G>A (p.Asp603Asn)
gnomAD v4
19g.41977983C>ACA406044974ATP1A3c.1935G>T (p.Glu645Asp)
c.1896G>T (p.Glu632Asp)
c.1929G>T (p.Glu643Asp)
c.1806G>T (p.Glu602Asp)
19g.41977983C>GCA406044975ATP1A3c.1935G>C (p.Glu645Asp)
c.1896G>C (p.Glu632Asp)
c.1929G>C (p.Glu643Asp)
c.1806G>C (p.Glu602Asp)
19g.41977983C>TCA507586487ATP1A3c.1935G>A (p.Glu645=)
c.1896G>A (p.Glu632=)
c.1929G>A (p.Glu643=)
c.1806G>A (p.Glu602=)
gnomAD v4
19g.41977984T>ACA406044976ATP1A3c.1934A>T (p.Glu645Val)
c.1895A>T (p.Glu632Val)
c.1928A>T (p.Glu643Val)
c.1805A>T (p.Glu602Val)
19g.41977984T>CCA406044978ATP1A3c.1934A>G (p.Glu645Gly)
c.1895A>G (p.Glu632Gly)
c.1928A>G (p.Glu643Gly)
c.1805A>G (p.Glu602Gly)
19g.41977984T>GCA406044977ATP1A3c.1934A>C (p.Glu645Ala)
c.1895A>C (p.Glu632Ala)
c.1928A>C (p.Glu643Ala)
c.1805A>C (p.Glu602Ala)
19g.41977985C>ACA406044979ATP1A3c.1933G>T (p.Glu645Ter)
c.1894G>T (p.Glu632Ter)
c.1927G>T (p.Glu643Ter)
c.1804G>T (p.Glu602Ter)
19g.41977985C>GCA406044980ATP1A3c.1933G>C (p.Glu645Gln)
c.1894G>C (p.Glu632Gln)
c.1927G>C (p.Glu643Gln)
c.1804G>C (p.Glu602Gln)
19g.41977985C>TCA406044981ATP1A3c.1933G>A (p.Glu645Lys)
c.1894G>A (p.Glu632Lys)
c.1927G>A (p.Glu643Lys)
c.1804G>A (p.Glu602Lys)
19g.41977986C>ACA507586500ATP1A3c.1932G>T (p.Val644=)
c.1893G>T (p.Val631=)
c.1926G>T (p.Val642=)
c.1803G>T (p.Val601=)
19g.41977986C>GCA507586502ATP1A3c.1932G>C (p.Val644=)
c.1893G>C (p.Val631=)
c.1926G>C (p.Val642=)
c.1803G>C (p.Val601=)
19g.41977986C>TCA507586504ATP1A3c.1932G>A (p.Val644=)
c.1893G>A (p.Val631=)
c.1926G>A (p.Val642=)
c.1803G>A (p.Val601=)
19g.41977987A>CCA406044982ATP1A3c.1931T>G (p.Val644Gly)
c.1892T>G (p.Val631Gly)
c.1925T>G (p.Val642Gly)
c.1802T>G (p.Val601Gly)
19g.41977987A>GCA406044983ATP1A3c.1931T>C (p.Val644Ala)
c.1892T>C (p.Val631Ala)
c.1925T>C (p.Val642Ala)
c.1802T>C (p.Val601Ala)
19g.41977987A>TCA406044984ATP1A3c.1931T>A (p.Val644Glu)
c.1892T>A (p.Val631Glu)
c.1925T>A (p.Val642Glu)
c.1802T>A (p.Val601Glu)
19g.41977988C>ACA406044985ATP1A3c.1930G>T (p.Val644Leu)
c.1891G>T (p.Val631Leu)
c.1924G>T (p.Val642Leu)
c.1801G>T (p.Val601Leu)
gnomAD v4
19g.41977988C>GCA406044986ATP1A3c.1930G>C (p.Val644Leu)
c.1891G>C (p.Val631Leu)
c.1924G>C (p.Val642Leu)
c.1801G>C (p.Val601Leu)
19g.41977988C>TCA406044988ATP1A3c.1930G>A (p.Val644Met)
c.1891G>A (p.Val631Met)
c.1924G>A (p.Val642Met)
c.1801G>A (p.Val601Met)
19g.41977989A=CA2336724838ATP1A3c.1929T= (p.Thr643=)
c.1890T= (p.Thr630=)
c.1923T= (p.Thr641=)
c.1800T= (p.Thr600=)
19g.41977989A>CCA507586517ATP1A3c.1929T>G (p.Thr643=)
c.1890T>G (p.Thr630=)
c.1923T>G (p.Thr641=)
c.1800T>G (p.Thr600=)
dbSNP
19g.41977989A>GCA9467544ATP1A3c.1929T>C (p.Thr643=)
c.1890T>C (p.Thr630=)
c.1923T>C (p.Thr641=)
c.1800T>C (p.Thr600=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.41977989A>TCA507586519ATP1A3c.1929T>A (p.Thr643=)
c.1890T>A (p.Thr630=)
c.1923T>A (p.Thr641=)
c.1800T>A (p.Thr600=)
19g.41977990G>ACA406044991ATP1A3c.1928C>T (p.Thr643Ile)
c.1889C>T (p.Thr630Ile)
c.1922C>T (p.Thr641Ile)
c.1799C>T (p.Thr600Ile)
19g.41977990G>CCA406044990ATP1A3c.1928C>G (p.Thr643Ser)
c.1889C>G (p.Thr630Ser)
c.1922C>G (p.Thr641Ser)
c.1799C>G (p.Thr600Ser)
19g.41977990G>TCA406044989ATP1A3c.1928C>A (p.Thr643Asn)
c.1889C>A (p.Thr630Asn)
c.1922C>A (p.Thr641Asn)
c.1799C>A (p.Thr600Asn)
19g.41977991T>ACA406044994ATP1A3c.1927A>T (p.Thr643Ser)
c.1888A>T (p.Thr630Ser)
c.1921A>T (p.Thr641Ser)
c.1798A>T (p.Thr600Ser)
19g.41977991T>CCA406044992ATP1A3c.1927A>G (p.Thr643Ala)
c.1888A>G (p.Thr630Ala)
c.1921A>G (p.Thr641Ala)
c.1798A>G (p.Thr600Ala)
19g.41977991T>GCA406044993ATP1A3c.1927A>C (p.Thr643Pro)
c.1888A>C (p.Thr630Pro)
c.1921A>C (p.Thr641Pro)
c.1798A>C (p.Thr600Pro)
19g.41977992C>ACA406044995ATP1A3c.1926G>T (p.Glu642Asp)
c.1887G>T (p.Glu629Asp)
c.1920G>T (p.Glu640Asp)
c.1797G>T (p.Glu599Asp)
19g.41977992C>GCA406044996ATP1A3c.1926G>C (p.Glu642Asp)
c.1887G>C (p.Glu629Asp)
c.1920G>C (p.Glu640Asp)
c.1797G>C (p.Glu599Asp)
19g.41977992C>TCA507586533ATP1A3c.1926G>A (p.Glu642=)
c.1887G>A (p.Glu629=)
c.1920G>A (p.Glu640=)
c.1797G>A (p.Glu599=)
19g.41977993T>ACA406044997ATP1A3c.1925A>T (p.Glu642Val)
c.1886A>T (p.Glu629Val)
c.1919A>T (p.Glu640Val)
c.1796A>T (p.Glu599Val)
19g.41977993T>CCA406044998ATP1A3c.1925A>G (p.Glu642Gly)
c.1886A>G (p.Glu629Gly)
c.1919A>G (p.Glu640Gly)
c.1796A>G (p.Glu599Gly)
19g.41977993T>GCA406044999ATP1A3c.1925A>C (p.Glu642Ala)
c.1886A>C (p.Glu629Ala)
c.1919A>C (p.Glu640Ala)
c.1796A>C (p.Glu599Ala)
19g.41977994C>ACA406045001ATP1A3c.1924G>T (p.Glu642Ter)
c.1885G>T (p.Glu629Ter)
c.1918G>T (p.Glu640Ter)
c.1795G>T (p.Glu599Ter)
19g.41977994C=CA2336724839ATP1A3c.1924G= (p.Glu642=)
c.1885G= (p.Glu629=)
c.1918G= (p.Glu640=)
c.1795G= (p.Glu599=)
19g.41977994C>GCA406045002ATP1A3c.1924G>C (p.Glu642Gln)
c.1885G>C (p.Glu629Gln)
c.1918G>C (p.Glu640Gln)
c.1795G>C (p.Glu599Gln)
19g.41977994C>TCA9467545ATP1A3c.1924G>A (p.Glu642Lys)
c.1885G>A (p.Glu629Lys)
c.1918G>A (p.Glu640Lys)
c.1795G>A (p.Glu599Lys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.41977995G>ACA9467546ATP1A3c.1923C>T (p.Asn641=)
c.1884C>T (p.Asn628=)
c.1917C>T (p.Asn639=)
c.1794C>T (p.Asn598=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41977995G>CCA406045003ATP1A3c.1923C>G (p.Asn641Lys)
c.1884C>G (p.Asn628Lys)
c.1917C>G (p.Asn639Lys)
c.1794C>G (p.Asn598Lys)
19g.41977995G=CA2336724840ATP1A3c.1923C= (p.Asn641=)
c.1884C= (p.Asn628=)
c.1917C= (p.Asn639=)
c.1794C= (p.Asn598=)
19g.41977995G>TCA406045004ATP1A3c.1923C>A (p.Asn641Lys)
c.1884C>A (p.Asn628Lys)
c.1917C>A (p.Asn639Lys)
c.1794C>A (p.Asn598Lys)
ClinVar dbSNP
19g.41977996T>ACA406045007ATP1A3c.1922A>T (p.Asn641Ile)
c.1883A>T (p.Asn628Ile)
c.1916A>T (p.Asn639Ile)
c.1793A>T (p.Asn598Ile)
19g.41977996T>CCA406045005ATP1A3c.1922A>G (p.Asn641Ser)
c.1883A>G (p.Asn628Ser)
c.1916A>G (p.Asn639Ser)
c.1793A>G (p.Asn598Ser)
19g.41977996T>GCA406045006ATP1A3c.1922A>C (p.Asn641Thr)
c.1883A>C (p.Asn628Thr)
c.1916A>C (p.Asn639Thr)
c.1793A>C (p.Asn598Thr)
19g.41977997T>ACA406045008ATP1A3c.1921A>T (p.Asn641Tyr)
c.1882A>T (p.Asn628Tyr)
c.1915A>T (p.Asn639Tyr)
c.1792A>T (p.Asn598Tyr)
19g.41977997T>CCA406045009ATP1A3c.1921A>G (p.Asn641Asp)
c.1882A>G (p.Asn628Asp)
c.1915A>G (p.Asn639Asp)
c.1792A>G (p.Asn598Asp)
19g.41977997T>GCA406045010ATP1A3c.1921A>C (p.Asn641His)
c.1882A>C (p.Asn628His)
c.1915A>C (p.Asn639His)
c.1792A>C (p.Asn598His)
19g.41977998G>ACA9467547ATP1A3c.1920C>T (p.Gly640=)
c.1881C>T (p.Gly627=)
c.1914C>T (p.Gly638=)
c.1791C>T (p.Gly597=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41977998G>CCA507586558ATP1A3c.1920C>G (p.Gly640=)
c.1881C>G (p.Gly627=)
c.1914C>G (p.Gly638=)
c.1791C>G (p.Gly597=)
19g.41977998G=CA2336724841ATP1A3c.1920C= (p.Gly640=)
c.1881C= (p.Gly627=)
c.1914C= (p.Gly638=)
c.1791C= (p.Gly597=)
19g.41977998G>TCA507586559ATP1A3c.1920C>A (p.Gly640=)
c.1881C>A (p.Gly627=)
c.1914C>A (p.Gly638=)
c.1791C>A (p.Gly597=)
19g.41977999C>ACA406045011ATP1A3c.1919G>T (p.Gly640Val)
c.1880G>T (p.Gly627Val)
c.1913G>T (p.Gly638Val)
c.1790G>T (p.Gly597Val)
19g.41977999C>GCA406045012ATP1A3c.1919G>C (p.Gly640Ala)
c.1880G>C (p.Gly627Ala)
c.1913G>C (p.Gly638Ala)
c.1790G>C (p.Gly597Ala)
19g.41977999C>TCA406045013ATP1A3c.1919G>A (p.Gly640Asp)
c.1880G>A (p.Gly627Asp)
c.1913G>A (p.Gly638Asp)
c.1790G>A (p.Gly597Asp)
19g.41978000C>ACA406045014ATP1A3c.1918G>T (p.Gly640Cys)
c.1879G>T (p.Gly627Cys)
c.1912G>T (p.Gly638Cys)
c.1789G>T (p.Gly597Cys)
19g.41978000C>GCA406045015ATP1A3c.1918G>C (p.Gly640Arg)
c.1879G>C (p.Gly627Arg)
c.1912G>C (p.Gly638Arg)
c.1789G>C (p.Gly597Arg)
19g.41978000C>TCA406045016ATP1A3c.1918G>A (p.Gly640Ser)
c.1879G>A (p.Gly627Ser)
c.1912G>A (p.Gly638Ser)
c.1789G>A (p.Gly597Ser)
19g.41978001C>ACA406045017ATP1A3c.1917G>T (p.Glu639Asp)
c.1878G>T (p.Glu626Asp)
c.1911G>T (p.Glu637Asp)
c.1788G>T (p.Glu596Asp)
19g.41978001C>GCA406045018ATP1A3c.1917G>C (p.Glu639Asp)
c.1878G>C (p.Glu626Asp)
c.1911G>C (p.Glu637Asp)
c.1788G>C (p.Glu596Asp)
19g.41978001C>TCA507586567ATP1A3c.1917G>A (p.Glu639=)
c.1878G>A (p.Glu626=)
c.1911G>A (p.Glu637=)
c.1788G>A (p.Glu596=)
19g.41978002T>ACA406045020ATP1A3c.1916A>T (p.Glu639Val)
c.1877A>T (p.Glu626Val)
c.1910A>T (p.Glu637Val)
c.1787A>T (p.Glu596Val)
19g.41978002T>CCA406045021ATP1A3c.1916A>G (p.Glu639Gly)
c.1877A>G (p.Glu626Gly)
c.1910A>G (p.Glu637Gly)
c.1787A>G (p.Glu596Gly)
19g.41978002T>GCA406045019ATP1A3c.1916A>C (p.Glu639Ala)
c.1877A>C (p.Glu626Ala)
c.1910A>C (p.Glu637Ala)
c.1787A>C (p.Glu596Ala)
19g.41978003C>ACA406045023ATP1A3c.1915G>T (p.Glu639Ter)
c.1876G>T (p.Glu626Ter)
c.1909G>T (p.Glu637Ter)
c.1786G>T (p.Glu596Ter)
19g.41978003C>GCA406045027ATP1A3c.1915G>C (p.Glu639Gln)
c.1876G>C (p.Glu626Gln)
c.1909G>C (p.Glu637Gln)
c.1786G>C (p.Glu596Gln)
19g.41978003C>TCA406045025ATP1A3c.1915G>A (p.Glu639Lys)
c.1876G>A (p.Glu626Lys)
c.1909G>A (p.Glu637Lys)
c.1786G>A (p.Glu596Lys)
19g.41978004A=CA2336724842ATP1A3c.1914T= (p.Ser638=)
c.1875T= (p.Ser625=)
c.1908T= (p.Ser636=)
c.1785T= (p.Ser595=)
19g.41978004A>CCA308591653ATP1A3c.1914T>G (p.Ser638=)
c.1875T>G (p.Ser625=)
c.1908T>G (p.Ser636=)
c.1785T>G (p.Ser595=)
dbSNP gnomAD v3 gnomAD v4
19g.41978004A>GCA507586581ATP1A3c.1914T>C (p.Ser638=)
c.1875T>C (p.Ser625=)
c.1908T>C (p.Ser636=)
c.1785T>C (p.Ser595=)
19g.41978004A>TCA507586583ATP1A3c.1914T>A (p.Ser638=)
c.1875T>A (p.Ser625=)
c.1908T>A (p.Ser636=)
c.1785T>A (p.Ser595=)
19g.41978005G>ACA406045030ATP1A3c.1913C>T (p.Ser638Phe)
c.1874C>T (p.Ser625Phe)
c.1907C>T (p.Ser636Phe)
c.1784C>T (p.Ser595Phe)
19g.41978005G>CCA406045031ATP1A3c.1913C>G (p.Ser638Cys)
c.1874C>G (p.Ser625Cys)
c.1907C>G (p.Ser636Cys)
c.1784C>G (p.Ser595Cys)
19g.41978005G>TCA406045033ATP1A3c.1913C>A (p.Ser638Tyr)
c.1874C>A (p.Ser625Tyr)
c.1907C>A (p.Ser636Tyr)
c.1784C>A (p.Ser595Tyr)
19g.41978006A>CCA406045035ATP1A3c.1912T>G (p.Ser638Ala)
c.1873T>G (p.Ser625Ala)
c.1906T>G (p.Ser636Ala)
c.1783T>G (p.Ser595Ala)
19g.41978006A>GCA406045037ATP1A3c.1912T>C (p.Ser638Pro)
c.1873T>C (p.Ser625Pro)
c.1906T>C (p.Ser636Pro)
c.1783T>C (p.Ser595Pro)
19g.41978006A>TCA406045038ATP1A3c.1912T>A (p.Ser638Thr)
c.1873T>A (p.Ser625Thr)
c.1906T>A (p.Ser636Thr)
c.1783T>A (p.Ser595Thr)
19g.41978007G>ACA507586594ATP1A3c.1911C>T (p.Ile637=)
c.1872C>T (p.Ile624=)
c.1905C>T (p.Ile635=)
c.1782C>T (p.Ile594=)
ClinVar dbSNP
19g.41978007G>CCA406045041ATP1A3c.1911C>G (p.Ile637Met)
c.1872C>G (p.Ile624Met)
c.1905C>G (p.Ile635Met)
c.1782C>G (p.Ile594Met)
19g.41978007G=CA2336724843ATP1A3c.1911C= (p.Ile637=)
c.1872C= (p.Ile624=)
c.1905C= (p.Ile635=)
c.1782C= (p.Ile594=)
19g.41978007G>TCA507586596ATP1A3c.1911C>A (p.Ile637=)
c.1872C>A (p.Ile624=)
c.1905C>A (p.Ile635=)
c.1782C>A (p.Ile594=)
19g.41978008A>CCA406045042ATP1A3c.1910T>G (p.Ile637Ser)
c.1871T>G (p.Ile624Ser)
c.1904T>G (p.Ile635Ser)
c.1781T>G (p.Ile594Ser)
19g.41978008A>GCA406045044ATP1A3c.1910T>C (p.Ile637Thr)
c.1871T>C (p.Ile624Thr)
c.1904T>C (p.Ile635Thr)
c.1781T>C (p.Ile594Thr)
19g.41978008A>TCA406045046ATP1A3c.1910T>A (p.Ile637Asn)
c.1871T>A (p.Ile624Asn)
c.1904T>A (p.Ile635Asn)
c.1781T>A (p.Ile594Asn)
ClinVar dbSNP
19g.41978009T>ACA406045052ATP1A3c.1909A>T (p.Ile637Phe)
c.1870A>T (p.Ile624Phe)
c.1903A>T (p.Ile635Phe)
c.1780A>T (p.Ile594Phe)
19g.41978009T>CCA406045050ATP1A3c.1909A>G (p.Ile637Val)
c.1870A>G (p.Ile624Val)
c.1903A>G (p.Ile635Val)
c.1780A>G (p.Ile594Val)
19g.41978009T>GCA406045048ATP1A3c.1909A>C (p.Ile637Leu)
c.1870A>C (p.Ile624Leu)
c.1903A>C (p.Ile635Leu)
c.1780A>C (p.Ile594Leu)
19g.41978010G>ACA9467548ATP1A3c.1908C>T (p.Ile636=)
c.1869C>T (p.Ile623=)
c.1902C>T (p.Ile634=)
c.1779C>T (p.Ile593=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.41978010G>CCA406045055ATP1A3c.1908C>G (p.Ile636Met)
c.1869C>G (p.Ile623Met)
c.1902C>G (p.Ile634Met)
c.1779C>G (p.Ile593Met)
19g.41978010G=CA2336724844ATP1A3c.1908C= (p.Ile636=)
c.1869C= (p.Ile623=)
c.1902C= (p.Ile634=)
c.1779C= (p.Ile593=)
19g.41978010G>TCA507586608ATP1A3c.1908C>A (p.Ile636=)
c.1869C>A (p.Ile623=)
c.1902C>A (p.Ile634=)
c.1779C>A (p.Ile593=)
19g.41978011A>CCA406045057ATP1A3c.1907T>G (p.Ile636Ser)
c.1868T>G (p.Ile623Ser)
c.1901T>G (p.Ile634Ser)
c.1778T>G (p.Ile593Ser)
19g.41978011A>GCA406045058ATP1A3c.1907T>C (p.Ile636Thr)
c.1868T>C (p.Ile623Thr)
c.1901T>C (p.Ile634Thr)
c.1778T>C (p.Ile593Thr)
19g.41978011A>TCA406045060ATP1A3c.1907T>A (p.Ile636Asn)
c.1868T>A (p.Ile623Asn)
c.1901T>A (p.Ile634Asn)
c.1778T>A (p.Ile593Asn)
19g.41978012T>ACA406045062ATP1A3c.1906A>T (p.Ile636Phe)
c.1867A>T (p.Ile623Phe)
c.1900A>T (p.Ile634Phe)
c.1777A>T (p.Ile593Phe)
19g.41978012T>CCA406045063ATP1A3c.1906A>G (p.Ile636Val)
c.1867A>G (p.Ile623Val)
c.1900A>G (p.Ile634Val)
c.1777A>G (p.Ile593Val)
19g.41978012T>GCA406045064ATP1A3c.1906A>C (p.Ile636Leu)
c.1867A>C (p.Ile623Leu)
c.1900A>C (p.Ile634Leu)
c.1777A>C (p.Ile593Leu)
19g.41978013G>ACA507586619ATP1A3c.1905C>T (p.Gly635=)
c.1866C>T (p.Gly622=)
c.1899C>T (p.Gly633=)
c.1776C>T (p.Gly592=)
19g.41978013G>CCA507586622ATP1A3c.1905C>G (p.Gly635=)
c.1866C>G (p.Gly622=)
c.1899C>G (p.Gly633=)
c.1776C>G (p.Gly592=)
19g.41978013G=CA2336724845ATP1A3c.1905C= (p.Gly635=)
c.1866C= (p.Gly622=)
c.1899C= (p.Gly633=)
c.1776C= (p.Gly592=)
19g.41978013G>TCA507586623ATP1A3c.1905C>A (p.Gly635=)
c.1866C>A (p.Gly622=)
c.1899C>A (p.Gly633=)
c.1776C>A (p.Gly592=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978014C>ACA406045065ATP1A3c.1904G>T (p.Gly635Val)
c.1865G>T (p.Gly622Val)
c.1898G>T (p.Gly633Val)
c.1775G>T (p.Gly592Val)
19g.41978014C>GCA406045066ATP1A3c.1904G>C (p.Gly635Ala)
c.1865G>C (p.Gly622Ala)
c.1898G>C (p.Gly633Ala)
c.1775G>C (p.Gly592Ala)
19g.41978014C>TCA406045068ATP1A3c.1904G>A (p.Gly635Asp)
c.1865G>A (p.Gly622Asp)
c.1898G>A (p.Gly633Asp)
c.1775G>A (p.Gly592Asp)
19g.41978015C>ACA406045074ATP1A3c.1903G>T (p.Gly635Cys)
c.1864G>T (p.Gly622Cys)
c.1897G>T (p.Gly633Cys)
c.1774G>T (p.Gly592Cys)
19g.41978015C>GCA406045072ATP1A3c.1903G>C (p.Gly635Arg)
c.1864G>C (p.Gly622Arg)
c.1897G>C (p.Gly633Arg)
c.1774G>C (p.Gly592Arg)
19g.41978015C>TCA406045071ATP1A3c.1903G>A (p.Gly635Ser)
c.1864G>A (p.Gly622Ser)
c.1897G>A (p.Gly633Ser)
c.1774G>A (p.Gly592Ser)
19g.41978016C>ACA507586635ATP1A3c.1902G>T (p.Val634=)
c.1863G>T (p.Val621=)
c.1896G>T (p.Val632=)
c.1773G>T (p.Val591=)
19g.41978016C>GCA507586636ATP1A3c.1902G>C (p.Val634=)
c.1863G>C (p.Val621=)
c.1896G>C (p.Val632=)
c.1773G>C (p.Val591=)
19g.41978016C>TCA507586638ATP1A3c.1902G>A (p.Val634=)
c.1863G>A (p.Val621=)
c.1896G>A (p.Val632=)
c.1773G>A (p.Val591=)
gnomAD v4
19g.41978017A>CCA406045077ATP1A3c.1901T>G (p.Val634Gly)
c.1862T>G (p.Val621Gly)
c.1895T>G (p.Val632Gly)
c.1772T>G (p.Val591Gly)
gnomAD v4
19g.41978017A>GCA406045078ATP1A3c.1901T>C (p.Val634Ala)
c.1862T>C (p.Val621Ala)
c.1895T>C (p.Val632Ala)
c.1772T>C (p.Val591Ala)
19g.41978017A>TCA406045079ATP1A3c.1901T>A (p.Val634Glu)
c.1862T>A (p.Val621Glu)
c.1895T>A (p.Val632Glu)
c.1772T>A (p.Val591Glu)
19g.41978018C>ACA406045081ATP1A3c.1900G>T (p.Val634Leu)
c.1861G>T (p.Val621Leu)
c.1894G>T (p.Val632Leu)
c.1771G>T (p.Val591Leu)
19g.41978018C>GCA406045082ATP1A3c.1900G>C (p.Val634Leu)
c.1861G>C (p.Val621Leu)
c.1894G>C (p.Val632Leu)
c.1771G>C (p.Val591Leu)
19g.41978018C>TCA406045085ATP1A3c.1900G>A (p.Val634Met)
c.1861G>A (p.Val621Met)
c.1894G>A (p.Val632Met)
c.1771G>A (p.Val591Met)
19g.41978019A=CA2336724846ATP1A3c.1899T= (p.Gly633=)
c.1860T= (p.Gly620=)
c.1893T= (p.Gly631=)
c.1770T= (p.Gly590=)
19g.41978019A>CCA507586647ATP1A3c.1899T>G (p.Gly633=)
c.1860T>G (p.Gly620=)
c.1893T>G (p.Gly631=)
c.1770T>G (p.Gly590=)
19g.41978019A>GCA507586649ATP1A3c.1899T>C (p.Gly633=)
c.1860T>C (p.Gly620=)
c.1893T>C (p.Gly631=)
c.1770T>C (p.Gly590=)
dbSNP gnomAD v3 gnomAD v4
19g.41978019A>TCA507586650ATP1A3c.1899T>A (p.Gly633=)
c.1860T>A (p.Gly620=)
c.1893T>A (p.Gly631=)
c.1770T>A (p.Gly590=)
19g.41978020C>ACA406045087ATP1A3c.1898G>T (p.Gly633Val)
c.1859G>T (p.Gly620Val)
c.1892G>T (p.Gly631Val)
c.1769G>T (p.Gly590Val)
19g.41978020C>GCA406045089ATP1A3c.1898G>C (p.Gly633Ala)
c.1859G>C (p.Gly620Ala)
c.1892G>C (p.Gly631Ala)
c.1769G>C (p.Gly590Ala)
19g.41978020C>TCA406045091ATP1A3c.1898G>A (p.Gly633Asp)
c.1859G>A (p.Gly620Asp)
c.1892G>A (p.Gly631Asp)
c.1769G>A (p.Gly590Asp)
19g.41978021C>ACA406045094ATP1A3c.1897G>T (p.Gly633Cys)
c.1858G>T (p.Gly620Cys)
c.1891G>T (p.Gly631Cys)
c.1768G>T (p.Gly590Cys)
19g.41978021C>GCA406045095ATP1A3c.1897G>C (p.Gly633Arg)
c.1858G>C (p.Gly620Arg)
c.1891G>C (p.Gly631Arg)
c.1768G>C (p.Gly590Arg)
19g.41978021C>TCA406045097ATP1A3c.1897G>A (p.Gly633Ser)
c.1858G>A (p.Gly620Ser)
c.1891G>A (p.Gly631Ser)
c.1768G>A (p.Gly590Ser)
19g.41978022C>ACA406045101ATP1A3c.1896G>T (p.Lys632Asn)
c.1857G>T (p.Lys619Asn)
c.1890G>T (p.Lys630Asn)
c.1767G>T (p.Lys589Asn)
COSMIC
19g.41978022C>GCA406045099ATP1A3c.1896G>C (p.Lys632Asn)
c.1857G>C (p.Lys619Asn)
c.1890G>C (p.Lys630Asn)
c.1767G>C (p.Lys589Asn)
19g.41978022C>TCA507586661ATP1A3c.1896G>A (p.Lys632=)
c.1857G>A (p.Lys619=)
c.1890G>A (p.Lys630=)
c.1767G>A (p.Lys589=)
19g.41978023T>ACA406045103ATP1A3c.1895A>T (p.Lys632Met)
c.1856A>T (p.Lys619Met)
c.1889A>T (p.Lys630Met)
c.1766A>T (p.Lys589Met)
19g.41978023T>CCA406045105ATP1A3c.1895A>G (p.Lys632Arg)
c.1856A>G (p.Lys619Arg)
c.1889A>G (p.Lys630Arg)
c.1766A>G (p.Lys589Arg)
19g.41978023T>GCA406045107ATP1A3c.1895A>C (p.Lys632Thr)
c.1856A>C (p.Lys619Thr)
c.1889A>C (p.Lys630Thr)
c.1766A>C (p.Lys589Thr)
19g.41978024T>ACA406045109ATP1A3c.1894A>T (p.Lys632Ter)
c.1855A>T (p.Lys619Ter)
c.1888A>T (p.Lys630Ter)
c.1765A>T (p.Lys589Ter)
19g.41978024T>CCA406045111ATP1A3c.1894A>G (p.Lys632Glu)
c.1855A>G (p.Lys619Glu)
c.1888A>G (p.Lys630Glu)
c.1765A>G (p.Lys589Glu)
19g.41978024T>GCA406045113ATP1A3c.1894A>C (p.Lys632Gln)
c.1855A>C (p.Lys619Gln)
c.1888A>C (p.Lys630Gln)
c.1765A>C (p.Lys589Gln)
19g.41978025G>ACA507586671ATP1A3c.1893C>T (p.Ala631=)
c.1854C>T (p.Ala618=)
c.1887C>T (p.Ala629=)
c.1764C>T (p.Ala588=)
ClinVar
19g.41978025G>CCA507586673ATP1A3c.1893C>G (p.Ala631=)
c.1854C>G (p.Ala618=)
c.1887C>G (p.Ala629=)
c.1764C>G (p.Ala588=)
19g.41978025G>TCA507586675ATP1A3c.1893C>A (p.Ala631=)
c.1854C>A (p.Ala618=)
c.1887C>A (p.Ala629=)
c.1764C>A (p.Ala588=)
19g.41978026G>ACA406045115ATP1A3c.1892C>T (p.Ala631Val)
c.1853C>T (p.Ala618Val)
c.1886C>T (p.Ala629Val)
c.1763C>T (p.Ala588Val)
ClinVar
19g.41978026G>CCA406045120ATP1A3c.1892C>G (p.Ala631Gly)
c.1853C>G (p.Ala618Gly)
c.1886C>G (p.Ala629Gly)
c.1763C>G (p.Ala588Gly)
19g.41978026G>TCA406045121ATP1A3c.1892C>A (p.Ala631Asp)
c.1853C>A (p.Ala618Asp)
c.1886C>A (p.Ala629Asp)
c.1763C>A (p.Ala588Asp)
ClinVar
19g.41978027C>ACA406045124ATP1A3c.1891G>T (p.Ala631Ser)
c.1852G>T (p.Ala618Ser)
c.1885G>T (p.Ala629Ser)
c.1762G>T (p.Ala588Ser)
19g.41978027C>GCA406045126ATP1A3c.1891G>C (p.Ala631Pro)
c.1852G>C (p.Ala618Pro)
c.1885G>C (p.Ala629Pro)
c.1762G>C (p.Ala588Pro)
19g.41978027C>TCA406045128ATP1A3c.1891G>A (p.Ala631Thr)
c.1852G>A (p.Ala618Thr)
c.1885G>A (p.Ala629Thr)
c.1762G>A (p.Ala588Thr)
19g.41978028A=CA2336724847ATP1A3c.1890T= (p.Ile630=)
c.1851T= (p.Ile617=)
c.1884T= (p.Ile628=)
c.1761T= (p.Ile587=)
19g.41978028A>CCA406045129ATP1A3c.1890T>G (p.Ile630Met)
c.1851T>G (p.Ile617Met)
c.1884T>G (p.Ile628Met)
c.1761T>G (p.Ile587Met)
19g.41978028A>GCA507586682ATP1A3c.1890T>C (p.Ile630=)
c.1851T>C (p.Ile617=)
c.1884T>C (p.Ile628=)
c.1761T>C (p.Ile587=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978028A>TCA507586683ATP1A3c.1890T>A (p.Ile630=)
c.1851T>A (p.Ile617=)
c.1884T>A (p.Ile628=)
c.1761T>A (p.Ile587=)
19g.41978029A>CCA406045131ATP1A3c.1889T>G (p.Ile630Ser)
c.1850T>G (p.Ile617Ser)
c.1883T>G (p.Ile628Ser)
c.1760T>G (p.Ile587Ser)
19g.41978029A>GCA406045134ATP1A3c.1889T>C (p.Ile630Thr)
c.1850T>C (p.Ile617Thr)
c.1883T>C (p.Ile628Thr)
c.1760T>C (p.Ile587Thr)
19g.41978029A>TCA406045130ATP1A3c.1889T>A (p.Ile630Asn)
c.1850T>A (p.Ile617Asn)
c.1883T>A (p.Ile628Asn)
c.1760T>A (p.Ile587Asn)
19g.41978030T>ACA406045140ATP1A3c.1888A>T (p.Ile630Phe)
c.1849A>T (p.Ile617Phe)
c.1882A>T (p.Ile628Phe)
c.1759A>T (p.Ile587Phe)
19g.41978030T>CCA406045137ATP1A3c.1888A>G (p.Ile630Val)
c.1849A>G (p.Ile617Val)
c.1882A>G (p.Ile628Val)
c.1759A>G (p.Ile587Val)
19g.41978030T>GCA406045138ATP1A3c.1888A>C (p.Ile630Leu)
c.1849A>C (p.Ile617Leu)
c.1882A>C (p.Ile628Leu)
c.1759A>C (p.Ile587Leu)
19g.41978031G>ACA507586694ATP1A3c.1887C>T (p.Ala629=)
c.1848C>T (p.Ala616=)
c.1881C>T (p.Ala627=)
c.1758C>T (p.Ala586=)
19g.41978031G>CCA507586693ATP1A3c.1887C>G (p.Ala629=)
c.1848C>G (p.Ala616=)
c.1881C>G (p.Ala627=)
c.1758C>G (p.Ala586=)
19g.41978031G>TCA507586690ATP1A3c.1887C>A (p.Ala629=)
c.1848C>A (p.Ala616=)
c.1881C>A (p.Ala627=)
c.1758C>A (p.Ala586=)
19g.41978032G>ACA406045142ATP1A3c.1886C>T (p.Ala629Val)
c.1847C>T (p.Ala616Val)
c.1880C>T (p.Ala627Val)
c.1757C>T (p.Ala586Val)
COSMIC
19g.41978032G>CCA406045144ATP1A3c.1886C>G (p.Ala629Gly)
c.1847C>G (p.Ala616Gly)
c.1880C>G (p.Ala627Gly)
c.1757C>G (p.Ala586Gly)
19g.41978032G>TCA406045145ATP1A3c.1886C>A (p.Ala629Asp)
c.1847C>A (p.Ala616Asp)
c.1880C>A (p.Ala627Asp)
c.1757C>A (p.Ala586Asp)
19g.41978033C>ACA406045148ATP1A3c.1885G>T (p.Ala629Ser)
c.1846G>T (p.Ala616Ser)
c.1879G>T (p.Ala627Ser)
c.1756G>T (p.Ala586Ser)
19g.41978033C>GCA406045150ATP1A3c.1885G>C (p.Ala629Pro)
c.1846G>C (p.Ala616Pro)
c.1879G>C (p.Ala627Pro)
c.1756G>C (p.Ala586Pro)
19g.41978033C>TCA406045151ATP1A3c.1885G>A (p.Ala629Thr)
c.1846G>A (p.Ala616Thr)
c.1879G>A (p.Ala627Thr)
c.1756G>A (p.Ala586Thr)
19g.41978034C>ACA406045153ATP1A3c.1884G>T (p.Lys628Asn)
c.1845G>T (p.Lys615Asn)
c.1878G>T (p.Lys626Asn)
c.1755G>T (p.Lys585Asn)
COSMIC
19g.41978034C>GCA406045155ATP1A3c.1884G>C (p.Lys628Asn)
c.1845G>C (p.Lys615Asn)
c.1878G>C (p.Lys626Asn)
c.1755G>C (p.Lys585Asn)
19g.41978034C>TCA507586707ATP1A3c.1884G>A (p.Lys628=)
c.1845G>A (p.Lys615=)
c.1878G>A (p.Lys626=)
c.1755G>A (p.Lys585=)
19g.41978035T>ACA406045157ATP1A3c.1883A>T (p.Lys628Met)
c.1844A>T (p.Lys615Met)
c.1877A>T (p.Lys626Met)
c.1754A>T (p.Lys585Met)
19g.41978035T>CCA406045158ATP1A3c.1883A>G (p.Lys628Arg)
c.1844A>G (p.Lys615Arg)
c.1877A>G (p.Lys626Arg)
c.1754A>G (p.Lys585Arg)
19g.41978035T>GCA406045160ATP1A3c.1883A>C (p.Lys628Thr)
c.1844A>C (p.Lys615Thr)
c.1877A>C (p.Lys626Thr)
c.1754A>C (p.Lys585Thr)
19g.41978036T>ACA406045168ATP1A3c.1882A>T (p.Lys628Ter)
c.1843A>T (p.Lys615Ter)
c.1876A>T (p.Lys626Ter)
c.1753A>T (p.Lys585Ter)
19g.41978036T>CCA406045163ATP1A3c.1882A>G (p.Lys628Glu)
c.1843A>G (p.Lys615Glu)
c.1876A>G (p.Lys626Glu)
c.1753A>G (p.Lys585Glu)
ClinVar
19g.41978036T>GCA406045164ATP1A3c.1882A>C (p.Lys628Gln)
c.1843A>C (p.Lys615Gln)
c.1876A>C (p.Lys626Gln)
c.1753A>C (p.Lys585Gln)
19g.41978037G>ACA507586718ATP1A3c.1881C>T (p.Ala627=)
c.1842C>T (p.Ala614=)
c.1875C>T (p.Ala625=)
c.1752C>T (p.Ala584=)
19g.41978037G>CCA507586719ATP1A3c.1881C>G (p.Ala627=)
c.1842C>G (p.Ala614=)
c.1875C>G (p.Ala625=)
c.1752C>G (p.Ala584=)
19g.41978037G>TCA507586721ATP1A3c.1881C>A (p.Ala627=)
c.1842C>A (p.Ala614=)
c.1875C>A (p.Ala625=)
c.1752C>A (p.Ala584=)
19g.41978038G>ACA406045173ATP1A3c.1880C>T (p.Ala627Val)
c.1841C>T (p.Ala614Val)
c.1874C>T (p.Ala625Val)
c.1751C>T (p.Ala584Val)
19g.41978038G>CCA406045175ATP1A3c.1880C>G (p.Ala627Gly)
c.1841C>G (p.Ala614Gly)
c.1874C>G (p.Ala625Gly)
c.1751C>G (p.Ala584Gly)
19g.41978038G>TCA406045176ATP1A3c.1880C>A (p.Ala627Asp)
c.1841C>A (p.Ala614Asp)
c.1874C>A (p.Ala625Asp)
c.1751C>A (p.Ala584Asp)
19g.41978039C>ACA406045178ATP1A3c.1879G>T (p.Ala627Ser)
c.1840G>T (p.Ala614Ser)
c.1873G>T (p.Ala625Ser)
c.1750G>T (p.Ala584Ser)
19g.41978039C>GCA406045181ATP1A3c.1879G>C (p.Ala627Pro)
c.1840G>C (p.Ala614Pro)
c.1873G>C (p.Ala625Pro)
c.1750G>C (p.Ala584Pro)
19g.41978039C>TCA406045182ATP1A3c.1879G>A (p.Ala627Thr)
c.1840G>A (p.Ala614Thr)
c.1873G>A (p.Ala625Thr)
c.1750G>A (p.Ala584Thr)
COSMIC
19g.41978040C>ACA507586735ATP1A3c.1878G>T (p.Thr626=)
c.1839G>T (p.Thr613=)
c.1872G>T (p.Thr624=)
c.1749G>T (p.Thr583=)
19g.41978040C=CA2336724848ATP1A3c.1878G= (p.Thr626=)
c.1839G= (p.Thr613=)
c.1872G= (p.Thr624=)
c.1749G= (p.Thr583=)
19g.41978040C>GCA507586737ATP1A3c.1878G>C (p.Thr626=)
c.1839G>C (p.Thr613=)
c.1872G>C (p.Thr624=)
c.1749G>C (p.Thr583=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978040C>TCA9467549ATP1A3c.1878G>A (p.Thr626=)
c.1839G>A (p.Thr613=)
c.1872G>A (p.Thr624=)
c.1749G>A (p.Thr583=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched