Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41978114G>ACA9467562ATP1A3c.1845+37C>T (n.1845+37C>T)
c.1806+37C>T (n.1806+37C>T)
c.1839+37C>T (n.1839+37C>T)
c.1716+37C>T (n.1716+37C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978114G>CCA9467563ATP1A3c.1845+37C>G (n.1845+37C>G)
c.1806+37C>G (n.1806+37C>G)
c.1839+37C>G (n.1839+37C>G)
c.1716+37C>G (n.1716+37C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978114G=CA2336724878ATP1A3c.1845+37C= (n.1845+37C=)
c.1806+37C= (n.1806+37C=)
c.1839+37C= (n.1839+37C=)
c.1716+37C= (n.1716+37C=)
19g.41978114G>TCA633185055ATP1A3c.1845+37C>A (n.1845+37C>A)
c.1806+37C>A (n.1806+37C>A)
c.1839+37C>A (n.1839+37C>A)
c.1716+37C>A (n.1716+37C>A)
 dbSNP gnomAD v2 gnomAD v4
19g.41978116C=CA2336724879ATP1A3c.1845+35G= (n.1845+35G=)
c.1806+35G= (n.1806+35G=)
c.1839+35G= (n.1839+35G=)
c.1716+35G= (n.1716+35G=)
19g.41978116C>GCA633185056ATP1A3c.1845+35G>C (n.1845+35G>C)
c.1806+35G>C (n.1806+35G>C)
c.1839+35G>C (n.1839+35G>C)
c.1716+35G>C (n.1716+35G>C)
 dbSNP gnomAD v2 gnomAD v4
19g.41978116C>TCA2521487290ATP1A3c.1845+35G>A (n.1845+35G>A)
c.1806+35G>A (n.1806+35G>A)
c.1839+35G>A (n.1839+35G>A)
c.1716+35G>A (n.1716+35G>A)
19g.41978119G>TCA2585369519ATP1A3c.1845+32C>A (n.1845+32C>A)
c.1806+32C>A (n.1806+32C>A)
c.1839+32C>A (n.1839+32C>A)
c.1716+32C>A (n.1716+32C>A)
 gnomAD v4
19g.41978119_41978120insGGCCCA2528967086ATP1A3c.1845+31_1845+32insGGCC (n.1845+31_1845+32insGGCC)
c.1806+31_1806+32insGGCC (n.1806+31_1806+32insGGCC)
c.1839+31_1839+32insGGCC (n.1839+31_1839+32insGGCC)
c.1716+31_1716+32insGGCC (n.1716+31_1716+32insGGCC)
19g.41978122_41978123insCTGGTCCCA2512950795ATP1A3c.1845+28_1845+29insGGACCAG (n.1845+28_1845+29insGGACCAG)
c.1806+28_1806+29insGGACCAG (n.1806+28_1806+29insGGACCAG)
c.1839+28_1839+29insGGACCAG (n.1839+28_1839+29insGGACCAG)
c.1716+28_1716+29insGGACCAG (n.1716+28_1716+29insGGACCAG)
19g.41978124G>ACA2814442099ATP1A3c.1845+27C>T (n.1845+27C>T)
c.1806+27C>T (n.1806+27C>T)
c.1839+27C>T (n.1839+27C>T)
c.1716+27C>T (n.1716+27C>T)
19g.41978124G>CCA2741632203ATP1A3c.1845+27C>G (n.1845+27C>G)
c.1806+27C>G (n.1806+27C>G)
c.1839+27C>G (n.1839+27C>G)
c.1716+27C>G (n.1716+27C>G)
19g.41978126C>ACA633185057ATP1A3c.1845+25G>T (n.1845+25G>T)
c.1806+25G>T (n.1806+25G>T)
c.1839+25G>T (n.1839+25G>T)
c.1716+25G>T (n.1716+25G>T)
 dbSNP gnomAD v2
19g.41978126C=CA2336724880ATP1A3c.1845+25G= (n.1845+25G=)
c.1806+25G= (n.1806+25G=)
c.1839+25G= (n.1839+25G=)
c.1716+25G= (n.1716+25G=)
19g.41978126C>GCA2585369520ATP1A3c.1845+25G>C (n.1845+25G>C)
c.1806+25G>C (n.1806+25G>C)
c.1839+25G>C (n.1839+25G>C)
c.1716+25G>C (n.1716+25G>C)
 gnomAD v4
19g.41978126C>TCA2585369521ATP1A3c.1845+25G>A (n.1845+25G>A)
c.1806+25G>A (n.1806+25G>A)
c.1839+25G>A (n.1839+25G>A)
c.1716+25G>A (n.1716+25G>A)
 gnomAD v4
19g.41978127T>CCA9467564ATP1A3c.1845+24A>G (n.1845+24A>G)
c.1806+24A>G (n.1806+24A>G)
c.1839+24A>G (n.1839+24A>G)
c.1716+24A>G (n.1716+24A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41978127T=CA2336724881ATP1A3c.1845+24A= (n.1845+24A=)
c.1806+24A= (n.1806+24A=)
c.1839+24A= (n.1839+24A=)
c.1716+24A= (n.1716+24A=)
19g.41978128C=CA2336724882ATP1A3c.1845+23G= (n.1845+23G=)
c.1806+23G= (n.1806+23G=)
c.1839+23G= (n.1839+23G=)
c.1716+23G= (n.1716+23G=)
19g.41978128C>TCA882387291ATP1A3c.1845+23G>A (n.1845+23G>A)
c.1806+23G>A (n.1806+23G>A)
c.1839+23G>A (n.1839+23G>A)
c.1716+23G>A (n.1716+23G>A)
 dbSNP gnomAD v3 gnomAD v4
19g.41978129C>GCA2576797161ATP1A3c.1845+22G>C (n.1845+22G>C)
c.1806+22G>C (n.1806+22G>C)
c.1839+22G>C (n.1839+22G>C)
c.1716+22G>C (n.1716+22G>C)
 gnomAD v4
19g.41978129C>TCA2585369522ATP1A3c.1845+22G>A (n.1845+22G>A)
c.1806+22G>A (n.1806+22G>A)
c.1839+22G>A (n.1839+22G>A)
c.1716+22G>A (n.1716+22G>A)
 gnomAD v4
19g.41978131_41978132insGGCA2548135082ATP1A3c.1845+19_1845+20insCC (n.1845+19_1845+20insCC)
c.1806+19_1806+20insCC (n.1806+19_1806+20insCC)
c.1839+19_1839+20insCC (n.1839+19_1839+20insCC)
c.1716+19_1716+20insCC (n.1716+19_1716+20insCC)
19g.41978132C>ACA2585369523ATP1A3c.1845+19G>T (n.1845+19G>T)
c.1806+19G>T (n.1806+19G>T)
c.1839+19G>T (n.1839+19G>T)
c.1716+19G>T (n.1716+19G>T)
 gnomAD v4
19g.41978132C=CA2336724883ATP1A3c.1845+19G= (n.1845+19G=)
c.1806+19G= (n.1806+19G=)
c.1839+19G= (n.1839+19G=)
c.1716+19G= (n.1716+19G=)
19g.41978132C>GCA2585369524ATP1A3c.1845+19G>C (n.1845+19G>C)
c.1806+19G>C (n.1806+19G>C)
c.1839+19G>C (n.1839+19G>C)
c.1716+19G>C (n.1716+19G>C)
 gnomAD v4
19g.41978132C>TCA633185058ATP1A3c.1845+19G>A (n.1845+19G>A)
c.1806+19G>A (n.1806+19G>A)
c.1839+19G>A (n.1839+19G>A)
c.1716+19G>A (n.1716+19G>A)
 dbSNP gnomAD v2 gnomAD v4
19g.41978133A=CA2336724884ATP1A3c.1845+18T= (n.1845+18T=)
c.1806+18T= (n.1806+18T=)
c.1839+18T= (n.1839+18T=)
c.1716+18T= (n.1716+18T=)
19g.41978133A>GCA9467565ATP1A3c.1845+18T>C (n.1845+18T>C)
c.1806+18T>C (n.1806+18T>C)
c.1839+18T>C (n.1839+18T>C)
c.1716+18T>C (n.1716+18T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41978134G>ACA2585369525ATP1A3c.1845+17C>T (n.1845+17C>T)
c.1806+17C>T (n.1806+17C>T)
c.1839+17C>T (n.1839+17C>T)
c.1716+17C>T (n.1716+17C>T)
 gnomAD v4
19g.41978134G>CCA2814442100ATP1A3c.1845+17C>G (n.1845+17C>G)
c.1806+17C>G (n.1806+17C>G)
c.1839+17C>G (n.1839+17C>G)
c.1716+17C>G (n.1716+17C>G)
19g.41978135C>TCA2814442101ATP1A3c.1845+16G>A (n.1845+16G>A)
c.1806+16G>A (n.1806+16G>A)
c.1839+16G>A (n.1839+16G>A)
c.1716+16G>A (n.1716+16G>A)
19g.41978137A=CA2336724885ATP1A3c.1845+14T= (n.1845+14T=)
c.1806+14T= (n.1806+14T=)
c.1839+14T= (n.1839+14T=)
c.1716+14T= (n.1716+14T=)
19g.41978137A>CCA9467566ATP1A3c.1845+14T>G (n.1845+14T>G)
c.1806+14T>G (n.1806+14T>G)
c.1839+14T>G (n.1839+14T>G)
c.1716+14T>G (n.1716+14T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978137A>GCA9467567ATP1A3c.1845+14T>C (n.1845+14T>C)
c.1806+14T>C (n.1806+14T>C)
c.1839+14T>C (n.1839+14T>C)
c.1716+14T>C (n.1716+14T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978138C=CA2336724886ATP1A3c.1845+13G= (n.1845+13G=)
c.1806+13G= (n.1806+13G=)
c.1839+13G= (n.1839+13G=)
c.1716+13G= (n.1716+13G=)
19g.41978138C>TCA633185059ATP1A3c.1845+13G>A (n.1845+13G>A)
c.1806+13G>A (n.1806+13G>A)
c.1839+13G>A (n.1839+13G>A)
c.1716+13G>A (n.1716+13G>A)
 dbSNP gnomAD v2 gnomAD v4
19g.41978139C=CA2336724887ATP1A3c.1845+12G= (n.1845+12G=)
c.1806+12G= (n.1806+12G=)
c.1839+12G= (n.1839+12G=)
c.1716+12G= (n.1716+12G=)
19g.41978139C>GCA633185060ATP1A3c.1845+12G>C (n.1845+12G>C)
c.1806+12G>C (n.1806+12G>C)
c.1839+12G>C (n.1839+12G>C)
c.1716+12G>C (n.1716+12G>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41978139C>TCA633185061ATP1A3c.1845+12G>A (n.1845+12G>A)
c.1806+12G>A (n.1806+12G>A)
c.1839+12G>A (n.1839+12G>A)
c.1716+12G>A (n.1716+12G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978140C=CA2336724888ATP1A3c.1845+11G= (n.1845+11G=)
c.1806+11G= (n.1806+11G=)
c.1839+11G= (n.1839+11G=)
c.1716+11G= (n.1716+11G=)
19g.41978140C>GCA633185062ATP1A3c.1845+11G>C (n.1845+11G>C)
c.1806+11G>C (n.1806+11G>C)
c.1839+11G>C (n.1839+11G>C)
c.1716+11G>C (n.1716+11G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978141C>ACA633185063ATP1A3c.1845+10G>T (n.1845+10G>T)
c.1806+10G>T (n.1806+10G>T)
c.1839+10G>T (n.1839+10G>T)
c.1716+10G>T (n.1716+10G>T)
 dbSNP gnomAD v2
19g.41978141C=CA2336724889ATP1A3c.1845+10G= (n.1845+10G=)
c.1806+10G= (n.1806+10G=)
c.1839+10G= (n.1839+10G=)
c.1716+10G= (n.1716+10G=)
19g.41978141C>TCA9467568ATP1A3c.1845+10G>A (n.1845+10G>A)
c.1806+10G>A (n.1806+10G>A)
c.1839+10G>A (n.1839+10G>A)
c.1716+10G>A (n.1716+10G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978144G>ACA2585369526ATP1A3c.1845+7C>T (n.1845+7C>T)
c.1806+7C>T (n.1806+7C>T)
c.1839+7C>T (n.1839+7C>T)
c.1716+7C>T (n.1716+7C>T)
 gnomAD v4
19g.41978144G>CCA633185064ATP1A3c.1845+7C>G (n.1845+7C>G)
c.1806+7C>G (n.1806+7C>G)
c.1839+7C>G (n.1839+7C>G)
c.1716+7C>G (n.1716+7C>G)
 dbSNP gnomAD v2 gnomAD v4
19g.41978144G=CA2336724890ATP1A3c.1845+7C= (n.1845+7C=)
c.1806+7C= (n.1806+7C=)
c.1839+7C= (n.1839+7C=)
c.1716+7C= (n.1716+7C=)
19g.41978145_41978146insACACCCAACA2814442102ATP1A3c.1845+5_1845+6insTTGGGTGT (n.1845+5_1845+6insTTGGGTGT)
c.1806+5_1806+6insTTGGGTGT (n.1806+5_1806+6insTTGGGTGT)
c.1839+5_1839+6insTTGGGTGT (n.1839+5_1839+6insTTGGGTGT)
c.1716+5_1716+6insTTGGGTGT (n.1716+5_1716+6insTTGGGTGT)
19g.41978147A>GCA2576797162ATP1A3c.1845+4T>C (n.1845+4T>C)
c.1806+4T>C (n.1806+4T>C)
c.1839+4T>C (n.1839+4T>C)
c.1716+4T>C (n.1716+4T>C)
 gnomAD v4
19g.41978148C>TCA2573156408ATP1A3c.1845+3G>A (n.1845+3G>A)
c.1806+3G>A (n.1806+3G>A)
c.1839+3G>A (n.1839+3G>A)
c.1716+3G>A (n.1716+3G>A)
 ClinVar dbSNP
19g.41978149A=CA2336724891ATP1A3c.1845+2T= (n.1845+2T=)
c.1806+2T= (n.1806+2T=)
c.1839+2T= (n.1839+2T=)
c.1716+2T= (n.1716+2T=)
19g.41978149A>CCA406045361ATP1A3c.1845+2T>G (n.1845+2T>G)
c.1806+2T>G (n.1806+2T>G)
c.1839+2T>G (n.1839+2T>G)
c.1716+2T>G (n.1716+2T>G)
19g.41978149A>GCA406045359ATP1A3c.1845+2T>C (n.1845+2T>C)
c.1806+2T>C (n.1806+2T>C)
c.1839+2T>C (n.1839+2T>C)
c.1716+2T>C (n.1716+2T>C)
 dbSNP
19g.41978149A>TCA406045357ATP1A3c.1845+2T>A (n.1845+2T>A)
c.1806+2T>A (n.1806+2T>A)
c.1839+2T>A (n.1839+2T>A)
c.1716+2T>A (n.1716+2T>A)
19g.41978150C>ACA406045365ATP1A3c.1845+1G>T (n.1845+1G>T)
c.1806+1G>T (n.1806+1G>T)
c.1839+1G>T (n.1839+1G>T)
c.1716+1G>T (n.1716+1G>T)
19g.41978150C>GCA406045364ATP1A3c.1845+1G>C (n.1845+1G>C)
c.1806+1G>C (n.1806+1G>C)
c.1839+1G>C (n.1839+1G>C)
c.1716+1G>C (n.1716+1G>C)
19g.41978150C>TCA406045367ATP1A3c.1845+1G>A (n.1845+1G>A)
c.1806+1G>A (n.1806+1G>A)
c.1839+1G>A (n.1839+1G>A)
c.1716+1G>A (n.1716+1G>A)
 COSMIC
19g.41978151C>ACA406045369ATP1A3c.1845G>T (p.Lys615Asn)
c.1806G>T (p.Lys602Asn)
c.1839G>T (p.Lys613Asn)
c.1716G>T (p.Lys572Asn)
19g.41978151C>GCA406045371ATP1A3c.1845G>C (p.Lys615Asn)
c.1806G>C (p.Lys602Asn)
c.1839G>C (p.Lys613Asn)
c.1716G>C (p.Lys572Asn)
19g.41978151C>TCA507586910ATP1A3c.1845G>A (p.Lys615=)
c.1806G>A (p.Lys602=)
c.1839G>A (p.Lys613=)
c.1716G>A (p.Lys572=)
19g.41978152T>ACA406045373ATP1A3c.1844A>T (p.Lys615Met)
c.1805A>T (p.Lys602Met)
c.1838A>T (p.Lys613Met)
c.1715A>T (p.Lys572Met)
19g.41978152T>CCA406045375ATP1A3c.1844A>G (p.Lys615Arg)
c.1805A>G (p.Lys602Arg)
c.1838A>G (p.Lys613Arg)
c.1715A>G (p.Lys572Arg)
19g.41978152T>GCA406045377ATP1A3c.1844A>C (p.Lys615Thr)
c.1805A>C (p.Lys602Thr)
c.1838A>C (p.Lys613Thr)
c.1715A>C (p.Lys572Thr)
19g.41978153T>ACA406045379ATP1A3c.1843A>T (p.Lys615Ter)
c.1804A>T (p.Lys602Ter)
c.1837A>T (p.Lys613Ter)
c.1714A>T (p.Lys572Ter)
19g.41978153T>CCA406045381ATP1A3c.1843A>G (p.Lys615Glu)
c.1804A>G (p.Lys602Glu)
c.1837A>G (p.Lys613Glu)
c.1714A>G (p.Lys572Glu)
19g.41978153T>GCA406045383ATP1A3c.1843A>C (p.Lys615Gln)
c.1804A>C (p.Lys602Gln)
c.1837A>C (p.Lys613Gln)
c.1714A>C (p.Lys572Gln)
19g.41978154G>ACA507586921ATP1A3c.1842C>T (p.Ile614=)
c.1803C>T (p.Ile601=)
c.1836C>T (p.Ile612=)
c.1713C>T (p.Ile571=)
 ClinVar gnomAD v4
19g.41978154G>CCA406045385ATP1A3c.1842C>G (p.Ile614Met)
c.1803C>G (p.Ile601Met)
c.1836C>G (p.Ile612Met)
c.1713C>G (p.Ile571Met)
19g.41978154G>TCA507586923ATP1A3c.1842C>A (p.Ile614=)
c.1803C>A (p.Ile601=)
c.1836C>A (p.Ile612=)
c.1713C>A (p.Ile571=)
19g.41978155A>CCA406045388ATP1A3c.1841T>G (p.Ile614Ser)
c.1802T>G (p.Ile601Ser)
c.1835T>G (p.Ile612Ser)
c.1712T>G (p.Ile571Ser)
19g.41978155A>GCA406045389ATP1A3c.1841T>C (p.Ile614Thr)
c.1802T>C (p.Ile601Thr)
c.1835T>C (p.Ile612Thr)
c.1712T>C (p.Ile571Thr)
19g.41978155A>TCA406045390ATP1A3c.1841T>A (p.Ile614Asn)
c.1802T>A (p.Ile601Asn)
c.1835T>A (p.Ile612Asn)
c.1712T>A (p.Ile571Asn)
19g.41978156T>ACA406045392ATP1A3c.1840A>T (p.Ile614Phe)
c.1801A>T (p.Ile601Phe)
c.1834A>T (p.Ile612Phe)
c.1711A>T (p.Ile571Phe)
 ClinVar dbSNP
19g.41978156T>CCA406045394ATP1A3c.1840A>G (p.Ile614Val)
c.1801A>G (p.Ile601Val)
c.1834A>G (p.Ile612Val)
c.1711A>G (p.Ile571Val)
19g.41978156T>GCA406045396ATP1A3c.1840A>C (p.Ile614Leu)
c.1801A>C (p.Ile601Leu)
c.1834A>C (p.Ile612Leu)
c.1711A>C (p.Ile571Leu)
 gnomAD v4
19g.41978156T=CA2336724892ATP1A3c.1840A= (p.Ile614=)
c.1801A= (p.Ile601=)
c.1834A= (p.Ile612=)
c.1711A= (p.Ile571=)
19g.41978157G>ACA507586939ATP1A3c.1839C>T (p.Gly613=)
c.1800C>T (p.Gly600=)
c.1833C>T (p.Gly611=)
c.1710C>T (p.Gly570=)
 gnomAD v4
19g.41978157G>CCA507586941ATP1A3c.1839C>G (p.Gly613=)
c.1800C>G (p.Gly600=)
c.1833C>G (p.Gly611=)
c.1710C>G (p.Gly570=)
19g.41978157G>TCA507586943ATP1A3c.1839C>A (p.Gly613=)
c.1800C>A (p.Gly600=)
c.1833C>A (p.Gly611=)
c.1710C>A (p.Gly570=)
19g.41978158C>ACA406045398ATP1A3c.1838G>T (p.Gly613Val)
c.1799G>T (p.Gly600Val)
c.1832G>T (p.Gly611Val)
c.1709G>T (p.Gly570Val)
19g.41978158C>GCA406045401ATP1A3c.1838G>C (p.Gly613Ala)
c.1799G>C (p.Gly600Ala)
c.1832G>C (p.Gly611Ala)
c.1709G>C (p.Gly570Ala)
19g.41978158C>TCA406045400ATP1A3c.1838G>A (p.Gly613Asp)
c.1799G>A (p.Gly600Asp)
c.1832G>A (p.Gly611Asp)
c.1709G>A (p.Gly570Asp)
 COSMIC
19g.41978159C>ACA406045402ATP1A3c.1837G>T (p.Gly613Cys)
c.1798G>T (p.Gly600Cys)
c.1831G>T (p.Gly611Cys)
c.1708G>T (p.Gly570Cys)
19g.41978159C>GCA406045404ATP1A3c.1837G>C (p.Gly613Arg)
c.1798G>C (p.Gly600Arg)
c.1831G>C (p.Gly611Arg)
c.1708G>C (p.Gly570Arg)
19g.41978159C>TCA406045406ATP1A3c.1837G>A (p.Gly613Ser)
c.1798G>A (p.Gly600Ser)
c.1831G>A (p.Gly611Ser)
c.1708G>A (p.Gly570Ser)
19g.41978160T>ACA507586965ATP1A3c.1836A>T (p.Ala612=)
c.1797A>T (p.Ala599=)
c.1830A>T (p.Ala610=)
c.1707A>T (p.Ala569=)
19g.41978160T>CCA507586967ATP1A3c.1836A>G (p.Ala612=)
c.1797A>G (p.Ala599=)
c.1830A>G (p.Ala610=)
c.1707A>G (p.Ala569=)
 dbSNP gnomAD v3 gnomAD v4
19g.41978160T>GCA507586969ATP1A3c.1836A>C (p.Ala612=)
c.1797A>C (p.Ala599=)
c.1830A>C (p.Ala610=)
c.1707A>C (p.Ala569=)
19g.41978161G>ACA406045409ATP1A3c.1835C>T (p.Ala612Val)
c.1796C>T (p.Ala599Val)
c.1829C>T (p.Ala610Val)
c.1706C>T (p.Ala569Val)
19g.41978161G>CCA406045410ATP1A3c.1835C>G (p.Ala612Gly)
c.1796C>G (p.Ala599Gly)
c.1829C>G (p.Ala610Gly)
c.1706C>G (p.Ala569Gly)
19g.41978161G>TCA406045412ATP1A3c.1835C>A (p.Ala612Glu)
c.1796C>A (p.Ala599Glu)
c.1829C>A (p.Ala610Glu)
c.1706C>A (p.Ala569Glu)
19g.41978162C>ACA406045414ATP1A3c.1834G>T (p.Ala612Ser)
c.1795G>T (p.Ala599Ser)
c.1828G>T (p.Ala610Ser)
c.1705G>T (p.Ala569Ser)
 gnomAD v4
19g.41978162C=CA2336724893ATP1A3c.1834G= (p.Ala612=)
c.1795G= (p.Ala599=)
c.1828G= (p.Ala610=)
c.1705G= (p.Ala569=)
19g.41978162C>GCA406045415ATP1A3c.1834G>C (p.Ala612Pro)
c.1795G>C (p.Ala599Pro)
c.1828G>C (p.Ala610Pro)
c.1705G>C (p.Ala569Pro)
 ClinVar
19g.41978162C>TCA16043749ATP1A3c.1834G>A (p.Ala612Thr)
c.1795G>A (p.Ala599Thr)
c.1828G>A (p.Ala610Thr)
c.1705G>A (p.Ala569Thr)
 ClinVar dbSNP gnomAD v4
19g.41978163G>ACA9467569ATP1A3c.1833C>T (p.Ser611=)
c.1794C>T (p.Ser598=)
c.1827C>T (p.Ser609=)
c.1704C>T (p.Ser568=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41978163G>CCA406045418ATP1A3c.1833C>G (p.Ser611Arg)
c.1794C>G (p.Ser598Arg)
c.1827C>G (p.Ser609Arg)
c.1704C>G (p.Ser568Arg)
19g.41978163G=CA2336724894ATP1A3c.1833C= (p.Ser611=)
c.1794C= (p.Ser598=)
c.1827C= (p.Ser609=)
c.1704C= (p.Ser568=)
19g.41978163G>TCA406045420ATP1A3c.1833C>A (p.Ser611Arg)
c.1794C>A (p.Ser598Arg)
c.1827C>A (p.Ser609Arg)
c.1704C>A (p.Ser568Arg)
19g.41978164C>ACA406045427ATP1A3c.1832G>T (p.Ser611Ile)
c.1793G>T (p.Ser598Ile)
c.1826G>T (p.Ser609Ile)
c.1703G>T (p.Ser568Ile)
19g.41978164C>GCA406045423ATP1A3c.1832G>C (p.Ser611Thr)
c.1793G>C (p.Ser598Thr)
c.1826G>C (p.Ser609Thr)
c.1703G>C (p.Ser568Thr)
19g.41978164C>TCA406045424ATP1A3c.1832G>A (p.Ser611Asn)
c.1793G>A (p.Ser598Asn)
c.1826G>A (p.Ser609Asn)
c.1703G>A (p.Ser568Asn)
19g.41978165T>ACA406045429ATP1A3c.1831A>T (p.Ser611Cys)
c.1792A>T (p.Ser598Cys)
c.1825A>T (p.Ser609Cys)
c.1702A>T (p.Ser568Cys)
19g.41978165T>CCA406045431ATP1A3c.1831A>G (p.Ser611Gly)
c.1792A>G (p.Ser598Gly)
c.1825A>G (p.Ser609Gly)
c.1702A>G (p.Ser568Gly)
19g.41978165T>GCA406045433ATP1A3c.1831A>C (p.Ser611Arg)
c.1792A>C (p.Ser598Arg)
c.1825A>C (p.Ser609Arg)
c.1702A>C (p.Ser568Arg)
19g.41978168_41978176delCA2580097322ATP1A3c.1823_1831del (p.Lys608_Arg610del)
c.1784_1792del (p.Lys595_Arg597del)
c.1817_1825del (p.Lys606_Arg608del)
c.1694_1702del (p.Lys565_Arg567del)
 ClinVar
19g.41978166G>ACA507694898ATP1A3c.1830C>T (p.Arg610=)
c.1791C>T (p.Arg597=)
c.1824C>T (p.Arg608=)
c.1701C>T (p.Arg567=)
19g.41978166G>CCA507694899ATP1A3c.1830C>G (p.Arg610=)
c.1791C>G (p.Arg597=)
c.1824C>G (p.Arg608=)
c.1701C>G (p.Arg567=)
19g.41978166G>TCA507694900ATP1A3c.1830C>A (p.Arg610=)
c.1791C>A (p.Arg597=)
c.1824C>A (p.Arg608=)
c.1701C>A (p.Arg567=)
19g.41978167C>ACA406045435ATP1A3c.1829G>T (p.Arg610Leu)
c.1790G>T (p.Arg597Leu)
c.1823G>T (p.Arg608Leu)
c.1700G>T (p.Arg567Leu)
19g.41978167C=CA2336724895ATP1A3c.1829G= (p.Arg610=)
c.1790G= (p.Arg597=)
c.1823G= (p.Arg608=)
c.1700G= (p.Arg567=)
19g.41978167C>GCA406045437ATP1A3c.1829G>C (p.Arg610Pro)
c.1790G>C (p.Arg597Pro)
c.1823G>C (p.Arg608Pro)
c.1700G>C (p.Arg567Pro)
19g.41978167C>TCA406045439ATP1A3c.1829G>A (p.Arg610His)
c.1790G>A (p.Arg597His)
c.1823G>A (p.Arg608His)
c.1700G>A (p.Arg567His)
 ClinVar dbSNP gnomAD v4
19g.41978168G>ACA406045444ATP1A3c.1828C>T (p.Arg610Cys)
c.1789C>T (p.Arg597Cys)
c.1822C>T (p.Arg608Cys)
c.1699C>T (p.Arg567Cys)
 ClinVar dbSNP
19g.41978168G>CCA406045442ATP1A3c.1828C>G (p.Arg610Gly)
c.1789C>G (p.Arg597Gly)
c.1822C>G (p.Arg608Gly)
c.1699C>G (p.Arg567Gly)
19g.41978168G=CA2336724896ATP1A3c.1828C= (p.Arg610=)
c.1789C= (p.Arg597=)
c.1822C= (p.Arg608=)
c.1699C= (p.Arg567=)
19g.41978168G>TCA406045443ATP1A3c.1828C>A (p.Arg610Ser)
c.1789C>A (p.Arg597Ser)
c.1822C>A (p.Arg608Ser)
c.1699C>A (p.Arg567Ser)
19g.41978169A>CCA406045447ATP1A3c.1827T>G (p.Cys609Trp)
c.1788T>G (p.Cys596Trp)
c.1821T>G (p.Cys607Trp)
c.1698T>G (p.Cys566Trp)
19g.41978169A>GCA507694905ATP1A3c.1827T>C (p.Cys609=)
c.1788T>C (p.Cys596=)
c.1821T>C (p.Cys607=)
c.1698T>C (p.Cys566=)
19g.41978169A>TCA406045449ATP1A3c.1827T>A (p.Cys609Ter)
c.1788T>A (p.Cys596Ter)
c.1821T>A (p.Cys607Ter)
c.1698T>A (p.Cys566Ter)
19g.41978170C>ACA406045451ATP1A3c.1826G>T (p.Cys609Phe)
c.1787G>T (p.Cys596Phe)
c.1820G>T (p.Cys607Phe)
c.1697G>T (p.Cys566Phe)
19g.41978170C>GCA406045453ATP1A3c.1826G>C (p.Cys609Ser)
c.1787G>C (p.Cys596Ser)
c.1820G>C (p.Cys607Ser)
c.1697G>C (p.Cys566Ser)
19g.41978170C>TCA406045455ATP1A3c.1826G>A (p.Cys609Tyr)
c.1787G>A (p.Cys596Tyr)
c.1820G>A (p.Cys607Tyr)
c.1697G>A (p.Cys566Tyr)
19g.41978171A>CCA406045457ATP1A3c.1825T>G (p.Cys609Gly)
c.1786T>G (p.Cys596Gly)
c.1819T>G (p.Cys607Gly)
c.1696T>G (p.Cys566Gly)
19g.41978171A>GCA406045461ATP1A3c.1825T>C (p.Cys609Arg)
c.1786T>C (p.Cys596Arg)
c.1819T>C (p.Cys607Arg)
c.1696T>C (p.Cys566Arg)
19g.41978171A>TCA406045460ATP1A3c.1825T>A (p.Cys609Ser)
c.1786T>A (p.Cys596Ser)
c.1819T>A (p.Cys607Ser)
c.1696T>A (p.Cys566Ser)
 gnomAD v4
19g.41978172C>ACA406045463ATP1A3c.1824G>T (p.Lys608Asn)
c.1785G>T (p.Lys595Asn)
c.1818G>T (p.Lys606Asn)
c.1695G>T (p.Lys565Asn)
19g.41978172C>GCA406045465ATP1A3c.1824G>C (p.Lys608Asn)
c.1785G>C (p.Lys595Asn)
c.1818G>C (p.Lys606Asn)
c.1695G>C (p.Lys565Asn)
19g.41978172C>TCA507694907ATP1A3c.1824G>A (p.Lys608=)
c.1785G>A (p.Lys595=)
c.1818G>A (p.Lys606=)
c.1695G>A (p.Lys565=)
 gnomAD v4
19g.41978173T>ACA406045468ATP1A3c.1823A>T (p.Lys608Met)
c.1784A>T (p.Lys595Met)
c.1817A>T (p.Lys606Met)
c.1694A>T (p.Lys565Met)
19g.41978173T>CCA406045469ATP1A3c.1823A>G (p.Lys608Arg)
c.1784A>G (p.Lys595Arg)
c.1817A>G (p.Lys606Arg)
c.1694A>G (p.Lys565Arg)
19g.41978173T>GCA406045470ATP1A3c.1823A>C (p.Lys608Thr)
c.1784A>C (p.Lys595Thr)
c.1817A>C (p.Lys606Thr)
c.1694A>C (p.Lys565Thr)
19g.41978174T>ACA406045473ATP1A3c.1822A>T (p.Lys608Ter)
c.1783A>T (p.Lys595Ter)
c.1816A>T (p.Lys606Ter)
c.1693A>T (p.Lys565Ter)
19g.41978174T>CCA406045475ATP1A3c.1822A>G (p.Lys608Glu)
c.1783A>G (p.Lys595Glu)
c.1816A>G (p.Lys606Glu)
c.1693A>G (p.Lys565Glu)
19g.41978174T>GCA406045477ATP1A3c.1822A>C (p.Lys608Gln)
c.1783A>C (p.Lys595Gln)
c.1816A>C (p.Lys606Gln)
c.1693A>C (p.Lys565Gln)
19g.41978175G>ACA507694908ATP1A3c.1821C>T (p.Gly607=)
c.1782C>T (p.Gly594=)
c.1815C>T (p.Gly605=)
c.1692C>T (p.Gly564=)
19g.41978175G>CCA507694910ATP1A3c.1821C>G (p.Gly607=)
c.1782C>G (p.Gly594=)
c.1815C>G (p.Gly605=)
c.1692C>G (p.Gly564=)
 gnomAD v4
19g.41978175G>TCA507694909ATP1A3c.1821C>A (p.Gly607=)
c.1782C>A (p.Gly594=)
c.1815C>A (p.Gly605=)
c.1692C>A (p.Gly564=)
19g.41978176C>ACA406045480ATP1A3c.1820G>T (p.Gly607Val)
c.1781G>T (p.Gly594Val)
c.1814G>T (p.Gly605Val)
c.1691G>T (p.Gly564Val)
19g.41978176C>GCA406045481ATP1A3c.1820G>C (p.Gly607Ala)
c.1781G>C (p.Gly594Ala)
c.1814G>C (p.Gly605Ala)
c.1691G>C (p.Gly564Ala)
 ClinVar dbSNP
19g.41978176C>TCA406045483ATP1A3c.1820G>A (p.Gly607Asp)
c.1781G>A (p.Gly594Asp)
c.1814G>A (p.Gly605Asp)
c.1691G>A (p.Gly564Asp)
19g.41978177C>ACA406045485ATP1A3c.1819G>T (p.Gly607Cys)
c.1780G>T (p.Gly594Cys)
c.1813G>T (p.Gly605Cys)
c.1690G>T (p.Gly564Cys)
19g.41978177C>GCA406045489ATP1A3c.1819G>C (p.Gly607Arg)
c.1780G>C (p.Gly594Arg)
c.1813G>C (p.Gly605Arg)
c.1690G>C (p.Gly564Arg)
19g.41978177C>TCA406045487ATP1A3c.1819G>A (p.Gly607Ser)
c.1780G>A (p.Gly594Ser)
c.1813G>A (p.Gly605Ser)
c.1690G>A (p.Gly564Ser)
19g.41978178C>ACA507694914ATP1A3c.1818G>T (p.Val606=)
c.1779G>T (p.Val593=)
c.1812G>T (p.Val604=)
c.1689G>T (p.Val563=)
19g.41978178C>GCA507694915ATP1A3c.1818G>C (p.Val606=)
c.1779G>C (p.Val593=)
c.1812G>C (p.Val604=)
c.1689G>C (p.Val563=)
19g.41978178C>TCA507694916ATP1A3c.1818G>A (p.Val606=)
c.1779G>A (p.Val593=)
c.1812G>A (p.Val604=)
c.1689G>A (p.Val563=)
 gnomAD v4
19g.41978179A>CCA406045491ATP1A3c.1817T>G (p.Val606Gly)
c.1778T>G (p.Val593Gly)
c.1811T>G (p.Val604Gly)
c.1688T>G (p.Val563Gly)
19g.41978179A>GCA406045496ATP1A3c.1817T>C (p.Val606Ala)
c.1778T>C (p.Val593Ala)
c.1811T>C (p.Val604Ala)
c.1688T>C (p.Val563Ala)
19g.41978179A>TCA406045493ATP1A3c.1817T>A (p.Val606Glu)
c.1778T>A (p.Val593Glu)
c.1811T>A (p.Val604Glu)
c.1688T>A (p.Val563Glu)
19g.41978180C>ACA406045498ATP1A3c.1816G>T (p.Val606Leu)
c.1777G>T (p.Val593Leu)
c.1810G>T (p.Val604Leu)
c.1687G>T (p.Val563Leu)
19g.41978180C>GCA406045500ATP1A3c.1816G>C (p.Val606Leu)
c.1777G>C (p.Val593Leu)
c.1810G>C (p.Val604Leu)
c.1687G>C (p.Val563Leu)
19g.41978180C>TCA406045502ATP1A3c.1816G>A (p.Val606Met)
c.1777G>A (p.Val593Met)
c.1810G>A (p.Val604Met)
c.1687G>A (p.Val563Met)
19g.41978181C>ACA507694920ATP1A3c.1815G>T (p.Ala605=)
c.1776G>T (p.Ala592=)
c.1809G>T (p.Ala603=)
c.1686G>T (p.Ala562=)
19g.41978181C=CA2336724897ATP1A3c.1815G= (p.Ala605=)
c.1776G= (p.Ala592=)
c.1809G= (p.Ala603=)
c.1686G= (p.Ala562=)
19g.41978181C>GCA507694922ATP1A3c.1815G>C (p.Ala605=)
c.1776G>C (p.Ala592=)
c.1809G>C (p.Ala603=)
c.1686G>C (p.Ala562=)
19g.41978181C>TCA9467570ATP1A3c.1815G>A (p.Ala605=)
c.1776G>A (p.Ala592=)
c.1809G>A (p.Ala603=)
c.1686G>A (p.Ala562=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978182G>ACA406045505ATP1A3c.1814C>T (p.Ala605Val)
c.1775C>T (p.Ala592Val)
c.1808C>T (p.Ala603Val)
c.1685C>T (p.Ala562Val)
 ClinVar dbSNP COSMIC
19g.41978182G>CCA406045507ATP1A3c.1814C>G (p.Ala605Gly)
c.1775C>G (p.Ala592Gly)
c.1808C>G (p.Ala603Gly)
c.1685C>G (p.Ala562Gly)
19g.41978182G=CA2336724898ATP1A3c.1814C= (p.Ala605=)
c.1775C= (p.Ala592=)
c.1808C= (p.Ala603=)
c.1685C= (p.Ala562=)
19g.41978182G>TCA406045509ATP1A3c.1814C>A (p.Ala605Glu)
c.1775C>A (p.Ala592Glu)
c.1808C>A (p.Ala603Glu)
c.1685C>A (p.Ala562Glu)
 ClinVar dbSNP
19g.41978183C>ACA406045511ATP1A3c.1813G>T (p.Ala605Ser)
c.1774G>T (p.Ala592Ser)
c.1807G>T (p.Ala603Ser)
c.1684G>T (p.Ala562Ser)
19g.41978183C>GCA406045512ATP1A3c.1813G>C (p.Ala605Pro)
c.1774G>C (p.Ala592Pro)
c.1807G>C (p.Ala603Pro)
c.1684G>C (p.Ala562Pro)
19g.41978183C>TCA406045515ATP1A3c.1813G>A (p.Ala605Thr)
c.1774G>A (p.Ala592Thr)
c.1807G>A (p.Ala603Thr)
c.1684G>A (p.Ala562Thr)
 gnomAD v4
19g.41978184G>ACA9467571ATP1A3c.1812C>T (p.Asp604=)
c.1773C>T (p.Asp591=)
c.1806C>T (p.Asp602=)
c.1683C>T (p.Asp561=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978184G>CCA406045518ATP1A3c.1812C>G (p.Asp604Glu)
c.1773C>G (p.Asp591Glu)
c.1806C>G (p.Asp602Glu)
c.1683C>G (p.Asp561Glu)
19g.41978184G=CA2336724899ATP1A3c.1812C= (p.Asp604=)
c.1773C= (p.Asp591=)
c.1806C= (p.Asp602=)
c.1683C= (p.Asp561=)
19g.41978184G>TCA406045520ATP1A3c.1812C>A (p.Asp604Glu)
c.1773C>A (p.Asp591Glu)
c.1806C>A (p.Asp602Glu)
c.1683C>A (p.Asp561Glu)
19g.41978185T>ACA406045522ATP1A3c.1811A>T (p.Asp604Val)
c.1772A>T (p.Asp591Val)
c.1805A>T (p.Asp602Val)
c.1682A>T (p.Asp561Val)
19g.41978185T>CCA406045526ATP1A3c.1811A>G (p.Asp604Gly)
c.1772A>G (p.Asp591Gly)
c.1805A>G (p.Asp602Gly)
c.1682A>G (p.Asp561Gly)
19g.41978185T>GCA406045524ATP1A3c.1811A>C (p.Asp604Ala)
c.1772A>C (p.Asp591Ala)
c.1805A>C (p.Asp602Ala)
c.1682A>C (p.Asp561Ala)
19g.41978186C>ACA406045528ATP1A3c.1810G>T (p.Asp604Tyr)
c.1771G>T (p.Asp591Tyr)
c.1804G>T (p.Asp602Tyr)
c.1681G>T (p.Asp561Tyr)
19g.41978186C>GCA406045529ATP1A3c.1810G>C (p.Asp604His)
c.1771G>C (p.Asp591His)
c.1804G>C (p.Asp602His)
c.1681G>C (p.Asp561His)
19g.41978186C>TCA406045531ATP1A3c.1810G>A (p.Asp604Asn)
c.1771G>A (p.Asp591Asn)
c.1804G>A (p.Asp602Asn)
c.1681G>A (p.Asp561Asn)
19g.41978187A>CCA507694927ATP1A3c.1809T>G (p.Pro603=)
c.1770T>G (p.Pro590=)
c.1803T>G (p.Pro601=)
c.1680T>G (p.Pro560=)
19g.41978187A>GCA507694930ATP1A3c.1809T>C (p.Pro603=)
c.1770T>C (p.Pro590=)
c.1803T>C (p.Pro601=)
c.1680T>C (p.Pro560=)
19g.41978187A>TCA507694929ATP1A3c.1809T>A (p.Pro603=)
c.1770T>A (p.Pro590=)
c.1803T>A (p.Pro601=)
c.1680T>A (p.Pro560=)
19g.41978188G>ACA406045533ATP1A3c.1808C>T (p.Pro603Leu)
c.1769C>T (p.Pro590Leu)
c.1802C>T (p.Pro601Leu)
c.1679C>T (p.Pro560Leu)
19g.41978188G>CCA406045535ATP1A3c.1808C>G (p.Pro603Arg)
c.1769C>G (p.Pro590Arg)
c.1802C>G (p.Pro601Arg)
c.1679C>G (p.Pro560Arg)
19g.41978188G>TCA406045536ATP1A3c.1808C>A (p.Pro603His)
c.1769C>A (p.Pro590His)
c.1802C>A (p.Pro601His)
c.1679C>A (p.Pro560His)
19g.41978189G>ACA406045539ATP1A3c.1807C>T (p.Pro603Ser)
c.1768C>T (p.Pro590Ser)
c.1801C>T (p.Pro601Ser)
c.1678C>T (p.Pro560Ser)
19g.41978189G>CCA406045541ATP1A3c.1807C>G (p.Pro603Ala)
c.1768C>G (p.Pro590Ala)
c.1801C>G (p.Pro601Ala)
c.1678C>G (p.Pro560Ala)
19g.41978189G>TCA406045543ATP1A3c.1807C>A (p.Pro603Thr)
c.1768C>A (p.Pro590Thr)
c.1801C>A (p.Pro601Thr)
c.1678C>A (p.Pro560Thr)
19g.41978190G>ACA507694933ATP1A3c.1806C>T (p.Val602=)
c.1767C>T (p.Val589=)
c.1800C>T (p.Val600=)
c.1677C>T (p.Val559=)
19g.41978190G>CCA507694934ATP1A3c.1806C>G (p.Val602=)
c.1767C>G (p.Val589=)
c.1800C>G (p.Val600=)
c.1677C>G (p.Val559=)
19g.41978190G=CA2336724900ATP1A3c.1806C= (p.Val602=)
c.1767C= (p.Val589=)
c.1800C= (p.Val600=)
c.1677C= (p.Val559=)
19g.41978190G>TCA507694935ATP1A3c.1806C>A (p.Val602=)
c.1767C>A (p.Val589=)
c.1800C>A (p.Val600=)
c.1677C>A (p.Val559=)
 dbSNP gnomAD v3 gnomAD v4
19g.41978191A>CCA406045549ATP1A3c.1805T>G (p.Val602Gly)
c.1766T>G (p.Val589Gly)
c.1799T>G (p.Val600Gly)
c.1676T>G (p.Val559Gly)
19g.41978191A>GCA406045547ATP1A3c.1805T>C (p.Val602Ala)
c.1766T>C (p.Val589Ala)
c.1799T>C (p.Val600Ala)
c.1676T>C (p.Val559Ala)
19g.41978191A>TCA406045545ATP1A3c.1805T>A (p.Val602Asp)
c.1766T>A (p.Val589Asp)
c.1799T>A (p.Val600Asp)
c.1676T>A (p.Val559Asp)
19g.41978192C>ACA406045551ATP1A3c.1804G>T (p.Val602Phe)
c.1765G>T (p.Val589Phe)
c.1798G>T (p.Val600Phe)
c.1675G>T (p.Val559Phe)
 ClinVar dbSNP
19g.41978192C=CA2336724901ATP1A3c.1804G= (p.Val602=)
c.1765G= (p.Val589=)
c.1798G= (p.Val600=)
c.1675G= (p.Val559=)
19g.41978192C>GCA406045553ATP1A3c.1804G>C (p.Val602Leu)
c.1765G>C (p.Val589Leu)
c.1798G>C (p.Val600Leu)
c.1675G>C (p.Val559Leu)
19g.41978192C>TCA406045555ATP1A3c.1804G>A (p.Val602Ile)
c.1765G>A (p.Val589Ile)
c.1798G>A (p.Val600Ile)
c.1675G>A (p.Val559Ile)
 gnomAD v4 COSMIC
19g.41978193G>ACA9467572ATP1A3c.1803C>T (p.Ala601=)
c.1764C>T (p.Ala588=)
c.1797C>T (p.Ala599=)
c.1674C>T (p.Ala558=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41978193G>CCA507694937ATP1A3c.1803C>G (p.Ala601=)
c.1764C>G (p.Ala588=)
c.1797C>G (p.Ala599=)
c.1674C>G (p.Ala558=)
 gnomAD v4
19g.41978193G=CA2336724902ATP1A3c.1803C= (p.Ala601=)
c.1764C= (p.Ala588=)
c.1797C= (p.Ala599=)
c.1674C= (p.Ala558=)
19g.41978193G>TCA507694939ATP1A3c.1803C>A (p.Ala601=)
c.1764C>A (p.Ala588=)
c.1797C>A (p.Ala599=)
c.1674C>A (p.Ala558=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41978194G>ACA406045558ATP1A3c.1802C>T (p.Ala601Val)
c.1763C>T (p.Ala588Val)
c.1796C>T (p.Ala599Val)
c.1673C>T (p.Ala558Val)
 dbSNP gnomAD v2 COSMIC
19g.41978194G>CCA406045560ATP1A3c.1802C>G (p.Ala601Gly)
c.1763C>G (p.Ala588Gly)
c.1796C>G (p.Ala599Gly)
c.1673C>G (p.Ala558Gly)
19g.41978194G=CA2336724903ATP1A3c.1802C= (p.Ala601=)
c.1763C= (p.Ala588=)
c.1796C= (p.Ala599=)
c.1673C= (p.Ala558=)
19g.41978194G>TCA406045562ATP1A3c.1802C>A (p.Ala601Asp)
c.1763C>A (p.Ala588Asp)
c.1796C>A (p.Ala599Asp)
c.1673C>A (p.Ala558Asp)
19g.41978195C>ACA406045565ATP1A3c.1801G>T (p.Ala601Ser)
c.1762G>T (p.Ala588Ser)
c.1795G>T (p.Ala599Ser)
c.1672G>T (p.Ala558Ser)
19g.41978195C>GCA406045566ATP1A3c.1801G>C (p.Ala601Pro)
c.1762G>C (p.Ala588Pro)
c.1795G>C (p.Ala599Pro)
c.1672G>C (p.Ala558Pro)
19g.41978195C>TCA406045568ATP1A3c.1801G>A (p.Ala601Thr)
c.1762G>A (p.Ala588Thr)
c.1795G>A (p.Ala599Thr)
c.1672G>A (p.Ala558Thr)
19g.41978196T>ACA507694945ATP1A3c.1800A>T (p.Ala600=)
c.1761A>T (p.Ala587=)
c.1794A>T (p.Ala598=)
c.1671A>T (p.Ala557=)
19g.41978196T>CCA507694943ATP1A3c.1800A>G (p.Ala600=)
c.1761A>G (p.Ala587=)
c.1794A>G (p.Ala598=)
c.1671A>G (p.Ala557=)
 dbSNP
19g.41978196T>GCA507694942ATP1A3c.1800A>C (p.Ala600=)
c.1761A>C (p.Ala587=)
c.1794A>C (p.Ala598=)
c.1671A>C (p.Ala557=)
19g.41978196T=CA2336724904ATP1A3c.1800A= (p.Ala600=)
c.1761A= (p.Ala587=)
c.1794A= (p.Ala598=)
c.1671A= (p.Ala557=)
19g.41978197G>ACA406045570ATP1A3c.1799C>T (p.Ala600Val)
c.1760C>T (p.Ala587Val)
c.1793C>T (p.Ala598Val)
c.1670C>T (p.Ala557Val)
19g.41978197G>CCA406045572ATP1A3c.1799C>G (p.Ala600Gly)
c.1760C>G (p.Ala587Gly)
c.1793C>G (p.Ala598Gly)
c.1670C>G (p.Ala557Gly)
19g.41978197G>TCA406045573ATP1A3c.1799C>A (p.Ala600Glu)
c.1760C>A (p.Ala587Glu)
c.1793C>A (p.Ala598Glu)
c.1670C>A (p.Ala557Glu)
19g.41978198C>ACA406045574ATP1A3c.1798G>T (p.Ala600Ser)
c.1759G>T (p.Ala587Ser)
c.1792G>T (p.Ala598Ser)
c.1669G>T (p.Ala557Ser)
19g.41978198C>GCA406045576ATP1A3c.1798G>C (p.Ala600Pro)
c.1759G>C (p.Ala587Pro)
c.1792G>C (p.Ala598Pro)
c.1669G>C (p.Ala557Pro)
19g.41978198C>TCA406045575ATP1A3c.1798G>A (p.Ala600Thr)
c.1759G>A (p.Ala587Thr)
c.1792G>A (p.Ala598Thr)
c.1669G>A (p.Ala557Thr)
19g.41978199C>ACA507694949ATP1A3c.1797G>T (p.Arg599=)
c.1758G>T (p.Arg586=)
c.1791G>T (p.Arg597=)
c.1668G>T (p.Arg556=)
19g.41978199C=CA2336724905ATP1A3c.1797G= (p.Arg599=)
c.1758G= (p.Arg586=)
c.1791G= (p.Arg597=)
c.1668G= (p.Arg556=)
19g.41978199C>GCA308591767ATP1A3c.1797G>C (p.Arg599=)
c.1758G>C (p.Arg586=)
c.1791G>C (p.Arg597=)
c.1668G>C (p.Arg556=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41978199C>TCA507694951ATP1A3c.1797G>A (p.Arg599=)
c.1758G>A (p.Arg586=)
c.1791G>A (p.Arg597=)
c.1668G>A (p.Arg556=)
19g.41978200C>ACA406045577ATP1A3c.1796G>T (p.Arg599Leu)
c.1757G>T (p.Arg586Leu)
c.1790G>T (p.Arg597Leu)
c.1667G>T (p.Arg556Leu)
19g.41978200C=CA2336724906ATP1A3c.1796G= (p.Arg599=)
c.1757G= (p.Arg586=)
c.1790G= (p.Arg597=)
c.1667G= (p.Arg556=)
19g.41978200C>GCA406045578ATP1A3c.1796G>C (p.Arg599Pro)
c.1757G>C (p.Arg586Pro)
c.1790G>C (p.Arg597Pro)
c.1667G>C (p.Arg556Pro)
19g.41978200C>TCA406045579ATP1A3c.1796G>A (p.Arg599Gln)
c.1757G>A (p.Arg586Gln)
c.1790G>A (p.Arg597Gln)
c.1667G>A (p.Arg556Gln)
 dbSNP
19g.41978201G>ACA406045580ATP1A3c.1795C>T (p.Arg599Trp)
c.1756C>T (p.Arg586Trp)
c.1789C>T (p.Arg597Trp)
c.1666C>T (p.Arg556Trp)
 ClinVar dbSNP gnomAD v2
19g.41978201G>CCA406045581ATP1A3c.1795C>G (p.Arg599Gly)
c.1756C>G (p.Arg586Gly)
c.1789C>G (p.Arg597Gly)
c.1666C>G (p.Arg556Gly)
19g.41978201G=CA2336724907ATP1A3c.1795C= (p.Arg599=)
c.1756C= (p.Arg586=)
c.1789C= (p.Arg597=)
c.1666C= (p.Arg556=)
19g.41978201G>TCA507694954ATP1A3c.1795C>A (p.Arg599=)
c.1756C>A (p.Arg586=)
c.1789C>A (p.Arg597=)
c.1666C>A (p.Arg556=)
 dbSNP
19g.41978202G>ACA507694955ATP1A3c.1794C>T (p.Pro598=)
c.1755C>T (p.Pro585=)
c.1788C>T (p.Pro596=)
c.1665C>T (p.Pro555=)
 ClinVar
19g.41978202G>CCA507694956ATP1A3c.1794C>G (p.Pro598=)
c.1755C>G (p.Pro585=)
c.1788C>G (p.Pro596=)
c.1665C>G (p.Pro555=)
 ClinVar gnomAD v4
19g.41978202G>TCA507694958ATP1A3c.1794C>A (p.Pro598=)
c.1755C>A (p.Pro585=)
c.1788C>A (p.Pro596=)
c.1665C>A (p.Pro555=)
19g.41978203G>ACA406045582ATP1A3c.1793C>T (p.Pro598Leu)
c.1754C>T (p.Pro585Leu)
c.1787C>T (p.Pro596Leu)
c.1664C>T (p.Pro555Leu)
19g.41978203G>CCA406045583ATP1A3c.1793C>G (p.Pro598Arg)
c.1754C>G (p.Pro585Arg)
c.1787C>G (p.Pro596Arg)
c.1664C>G (p.Pro555Arg)
19g.41978203G>TCA406045584ATP1A3c.1793C>A (p.Pro598His)
c.1754C>A (p.Pro585His)
c.1787C>A (p.Pro596His)
c.1664C>A (p.Pro555His)
19g.41978204G>ACA406045585ATP1A3c.1792C>T (p.Pro598Ser)
c.1753C>T (p.Pro585Ser)
c.1786C>T (p.Pro596Ser)
c.1663C>T (p.Pro555Ser)
19g.41978204G>CCA406045586ATP1A3c.1792C>G (p.Pro598Ala)
c.1753C>G (p.Pro585Ala)
c.1786C>G (p.Pro596Ala)
c.1663C>G (p.Pro555Ala)
19g.41978204G>TCA406045587ATP1A3c.1792C>A (p.Pro598Thr)
c.1753C>A (p.Pro585Thr)
c.1786C>A (p.Pro596Thr)
c.1663C>A (p.Pro555Thr)
19g.41978205T>ACA507694961ATP1A3c.1791A>T (p.Pro597=)
c.1752A>T (p.Pro584=)
c.1785A>T (p.Pro595=)
c.1662A>T (p.Pro554=)
19g.41978205T>CCA507694962ATP1A3c.1791A>G (p.Pro597=)
c.1752A>G (p.Pro584=)
c.1785A>G (p.Pro595=)
c.1662A>G (p.Pro554=)
19g.41978205T>GCA507694963ATP1A3c.1791A>C (p.Pro597=)
c.1752A>C (p.Pro584=)
c.1785A>C (p.Pro595=)
c.1662A>C (p.Pro554=)
19g.41978206G>ACA406045589ATP1A3c.1790C>T (p.Pro597Leu)
c.1751C>T (p.Pro584Leu)
c.1784C>T (p.Pro595Leu)
c.1661C>T (p.Pro554Leu)
19g.41978206G>CCA406045590ATP1A3c.1790C>G (p.Pro597Arg)
c.1751C>G (p.Pro584Arg)
c.1784C>G (p.Pro595Arg)
c.1661C>G (p.Pro554Arg)
19g.41978206G>TCA406045588ATP1A3c.1790C>A (p.Pro597Gln)
c.1751C>A (p.Pro584Gln)
c.1784C>A (p.Pro595Gln)
c.1661C>A (p.Pro554Gln)
19g.41978207G>ACA406045593ATP1A3c.1789C>T (p.Pro597Ser)
c.1750C>T (p.Pro584Ser)
c.1783C>T (p.Pro595Ser)
c.1660C>T (p.Pro554Ser)
19g.41978207G>CCA406045591ATP1A3c.1789C>G (p.Pro597Ala)
c.1750C>G (p.Pro584Ala)
c.1783C>G (p.Pro595Ala)
c.1660C>G (p.Pro554Ala)
19g.41978207G>TCA406045592ATP1A3c.1789C>A (p.Pro597Thr)
c.1750C>A (p.Pro584Thr)
c.1783C>A (p.Pro595Thr)
c.1660C>A (p.Pro554Thr)
19g.41978208G>ACA507694964ATP1A3c.1788C>T (p.Asp596=)
c.1749C>T (p.Asp583=)
c.1782C>T (p.Asp594=)
c.1659C>T (p.Asp553=)
19g.41978208G>CCA406045594ATP1A3c.1788C>G (p.Asp596Glu)
c.1749C>G (p.Asp583Glu)
c.1782C>G (p.Asp594Glu)
c.1659C>G (p.Asp553Glu)
19g.41978208G>TCA406045595ATP1A3c.1788C>A (p.Asp596Glu)
c.1749C>A (p.Asp583Glu)
c.1782C>A (p.Asp594Glu)
c.1659C>A (p.Asp553Glu)
19g.41978209T>ACA406045596ATP1A3c.1787A>T (p.Asp596Val)
c.1748A>T (p.Asp583Val)
c.1781A>T (p.Asp594Val)
c.1658A>T (p.Asp553Val)
19g.41978209T>CCA308591768ATP1A3c.1787A>G (p.Asp596Gly)
c.1748A>G (p.Asp583Gly)
c.1781A>G (p.Asp594Gly)
c.1658A>G (p.Asp553Gly)
 dbSNP
19g.41978209T>GCA406045597ATP1A3c.1787A>C (p.Asp596Ala)
c.1748A>C (p.Asp583Ala)
c.1781A>C (p.Asp594Ala)
c.1658A>C (p.Asp553Ala)
19g.41978209T=CA2336724908ATP1A3c.1787A= (p.Asp596=)
c.1748A= (p.Asp583=)
c.1781A= (p.Asp594=)
c.1658A= (p.Asp553=)
19g.41978210C>ACA406045602ATP1A3c.1786G>T (p.Asp596Tyr)
c.1747G>T (p.Asp583Tyr)
c.1780G>T (p.Asp594Tyr)
c.1657G>T (p.Asp553Tyr)
19g.41978210C>GCA406045599ATP1A3c.1786G>C (p.Asp596His)
c.1747G>C (p.Asp583His)
c.1780G>C (p.Asp594His)
c.1657G>C (p.Asp553His)
19g.41978210C>TCA406045600ATP1A3c.1786G>A (p.Asp596Asn)
c.1747G>A (p.Asp583Asn)
c.1780G>A (p.Asp594Asn)
c.1657G>A (p.Asp553Asn)
 ClinVar dbSNP
19g.41978211G>ACA9467573ATP1A3c.1785C>T (p.Ile595=)
c.1746C>T (p.Ile582=)
c.1779C>T (p.Ile593=)
c.1656C>T (p.Ile552=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41978211G>CCA406045604ATP1A3c.1785C>G (p.Ile595Met)
c.1746C>G (p.Ile582Met)
c.1779C>G (p.Ile593Met)
c.1656C>G (p.Ile552Met)
19g.41978211G=CA2336724909ATP1A3c.1785C= (p.Ile595=)
c.1746C= (p.Ile582=)
c.1779C= (p.Ile593=)
c.1656C= (p.Ile552=)
19g.41978211G>TCA507694969ATP1A3c.1785C>A (p.Ile595=)
c.1746C>A (p.Ile582=)
c.1779C>A (p.Ile593=)
c.1656C>A (p.Ile552=)
19g.41978212A>CCA406045607ATP1A3c.1784T>G (p.Ile595Ser)
c.1745T>G (p.Ile582Ser)
c.1778T>G (p.Ile593Ser)
c.1655T>G (p.Ile552Ser)
19g.41978212A>GCA406045608ATP1A3c.1784T>C (p.Ile595Thr)
c.1745T>C (p.Ile582Thr)
c.1778T>C (p.Ile593Thr)
c.1655T>C (p.Ile552Thr)
19g.41978212A>TCA406045610ATP1A3c.1784T>A (p.Ile595Asn)
c.1745T>A (p.Ile582Asn)
c.1778T>A (p.Ile593Asn)
c.1655T>A (p.Ile552Asn)
19g.41978213T>ACA406045613ATP1A3c.1783A>T (p.Ile595Phe)
c.1744A>T (p.Ile582Phe)
c.1777A>T (p.Ile593Phe)
c.1654A>T (p.Ile552Phe)
19g.41978213T>CCA406045616ATP1A3c.1783A>G (p.Ile595Val)
c.1744A>G (p.Ile582Val)
c.1777A>G (p.Ile593Val)
c.1654A>G (p.Ile552Val)
19g.41978213T>GCA406045614ATP1A3c.1783A>C (p.Ile595Leu)
c.1744A>C (p.Ile582Leu)
c.1777A>C (p.Ile593Leu)
c.1654A>C (p.Ile552Leu)
19g.41978214C>ACA406045618ATP1A3c.1782G>T (p.Met594Ile)
c.1743G>T (p.Met581Ile)
c.1776G>T (p.Met592Ile)
c.1653G>T (p.Met551Ile)
19g.41978214C>GCA406045620ATP1A3c.1782G>C (p.Met594Ile)
c.1743G>C (p.Met581Ile)
c.1776G>C (p.Met592Ile)
c.1653G>C (p.Met551Ile)
19g.41978214C>TCA406045622ATP1A3c.1782G>A (p.Met594Ile)
c.1743G>A (p.Met581Ile)
c.1776G>A (p.Met592Ile)
c.1653G>A (p.Met551Ile)

Number of alleles fetched