Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.28900564_28900565delCA719739897ATP2A1c.1765-17_1765-16del (n.1765-17_1765-16del)
c.1390-17_1390-16del (n.1390-17_1390-16del)
c.794-17_794-16del
 dbSNP gnomAD v3 gnomAD v4
16g.28900564C>ACA2632539719ATP2A1c.1765-17C>A (n.1765-17C>A)
c.1390-17C>A (n.1390-17C>A)
c.794-17C>A
 gnomAD v4
16g.28900564C>GCA2632539721ATP2A1c.1765-17C>G (n.1765-17C>G)
c.1390-17C>G (n.1390-17C>G)
c.794-17C>G
 gnomAD v4
16g.28900564_28900565insCAAGTTCACA2732138541ATP2A1c.1765-17_1765-16insCAAGTTCA (n.1765-17_1765-16insCAAGTTCA)
c.1390-17_1390-16insCAAGTTCA (n.1390-17_1390-16insCAAGTTCA)
c.794-17_794-16insCAAGTTCA
 dbSNP
16g.28900566G>ACA2632539722ATP2A1c.1765-15G>A (n.1765-15G>A)
c.1390-15G>A (n.1390-15G>A)
c.794-15G>A
 gnomAD v4
16g.28900566G>TCA2632539724ATP2A1c.1765-15G>T (n.1765-15G>T)
c.1390-15G>T (n.1390-15G>T)
c.794-15G>T
 gnomAD v4
16g.28900567C>ACA2215884191ATP2A1c.1765-14C>A (n.1765-14C>A)
c.1390-14C>A (n.1390-14C>A)
c.794-14C>A
 dbSNP gnomAD v4
16g.28900567C=CA2215884188ATP2A1c.1765-14C= (n.1765-14C=)
c.1390-14C= (n.1390-14C=)
c.794-14C=
16g.28900567C>GCA2731904219ATP2A1c.1765-14C>G (n.1765-14C>G)
c.1390-14C>G (n.1390-14C>G)
c.794-14C>G
 dbSNP
16g.28900567C>TCA621792659ATP2A1c.1765-14C>T (n.1765-14C>T)
c.1390-14C>T (n.1390-14C>T)
c.794-14C>T
 dbSNP gnomAD v2 gnomAD v4
16g.28900568T>ACA2731886977ATP2A1c.1765-13T>A (n.1765-13T>A)
c.1390-13T>A (n.1390-13T>A)
c.794-13T>A
 dbSNP
16g.28900568T>CCA621792662ATP2A1c.1765-13T>C (n.1765-13T>C)
c.1390-13T>C (n.1390-13T>C)
c.794-13T>C
 dbSNP gnomAD v2 gnomAD v4
16g.28900568T>GCA279239973ATP2A1c.1765-13T>G (n.1765-13T>G)
c.1390-13T>G (n.1390-13T>G)
c.794-13T>G
 dbSNP
16g.28900568T=CA2215884197ATP2A1c.1765-13T= (n.1765-13T=)
c.1390-13T= (n.1390-13T=)
c.794-13T=
16g.28900569G>ACA7987075ATP2A1c.1765-12G>A (n.1765-12G>A)
c.1390-12G>A (n.1390-12G>A)
c.794-12G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900569G>CCA7987076ATP2A1c.1765-12G>C (n.1765-12G>C)
c.1390-12G>C (n.1390-12G>C)
c.794-12G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900569G=CA2215884207ATP2A1c.1765-12G= (n.1765-12G=)
c.1390-12G= (n.1390-12G=)
c.794-12G=
16g.28900569G>TCA2632539734ATP2A1c.1765-12G>T (n.1765-12G>T)
c.1390-12G>T (n.1390-12G>T)
c.794-12G>T
 gnomAD v4
16g.28900570T>CCA2632539737ATP2A1c.1765-11T>C (n.1765-11T>C)
c.1390-11T>C (n.1390-11T>C)
c.794-11T>C
 gnomAD v4
16g.28900570dupCA621792667ATP2A1c.1765-11dup (n.1765-11dup)
c.1390-11dup (n.1390-11dup)
c.794-11dup
 dbSNP gnomAD v2 gnomAD v4
16g.28900570_28900571insCCCA2632539739ATP2A1c.1765-11_1765-10insCC (n.1765-11_1765-10insCC)
c.1390-11_1390-10insCC (n.1390-11_1390-10insCC)
c.794-11_794-10insCC
 gnomAD v4
16g.28900571A=CA2215884216ATP2A1c.1765-10A= (n.1765-10A=)
c.1390-10A= (n.1390-10A=)
c.794-10A=
16g.28900571A>GCA7987077ATP2A1c.1765-10A>G (n.1765-10A>G)
c.1390-10A>G (n.1390-10A>G)
c.794-10A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900572T>ACA2215884223ATP2A1c.1765-9T>A (n.1765-9T>A)
c.1390-9T>A (n.1390-9T>A)
c.794-9T>A
 dbSNP
16g.28900572T=CA2215884221ATP2A1c.1765-9T= (n.1765-9T=)
c.1390-9T= (n.1390-9T=)
c.794-9T=
16g.28900572_28900576delCA2732138543ATP2A1c.1765-9_1765-5del (n.1765-9_1765-5del)
c.1390-9_1390-5del (n.1390-9_1390-5del)
c.794-9_794-5del
 dbSNP
16g.28900574delCA2575960506ATP2A1c.1765-7del (n.1765-7del)
c.1390-7del (n.1390-7del)
c.794-7del
16g.28900574T>CCA2632539744ATP2A1c.1765-7T>C (n.1765-7T>C)
c.1390-7T>C (n.1390-7T>C)
c.794-7T>C
 gnomAD v4
16g.28900575C>ACA2632539745ATP2A1c.1765-6C>A (n.1765-6C>A)
c.1390-6C>A (n.1390-6C>A)
c.794-6C>A
 gnomAD v4
16g.28900575C=CA2215884232ATP2A1c.1765-6C= (n.1765-6C=)
c.1390-6C= (n.1390-6C=)
c.794-6C=
16g.28900575C>TCA621792670ATP2A1c.1765-6C>T (n.1765-6C>T)
c.1390-6C>T (n.1390-6C>T)
c.794-6C>T
 dbSNP gnomAD v2 gnomAD v4
16g.28900578delCA2806424055ATP2A1c.1765-3del (n.1765-3del)
c.1390-3del (n.1390-3del)
c.794-3del
16g.28900576C>ACA2632539747ATP2A1c.1765-5C>A (n.1765-5C>A)
c.1390-5C>A (n.1390-5C>A)
c.794-5C>A
 gnomAD v4
16g.28900577C>ACA2632539751ATP2A1c.1765-4C>A (n.1765-4C>A)
c.1390-4C>A (n.1390-4C>A)
c.794-4C>A
 gnomAD v4
16g.28900577C=CA2215884245ATP2A1c.1765-4C= (n.1765-4C=)
c.1390-4C= (n.1390-4C=)
c.794-4C=
16g.28900577C>GCA7987078ATP2A1c.1765-4C>G (n.1765-4C>G)
c.1390-4C>G (n.1390-4C>G)
c.794-4C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900578C>ACA2632539758ATP2A1c.1765-3C>A (n.1765-3C>A)
c.1390-3C>A (n.1390-3C>A)
c.794-3C>A
 gnomAD v4
16g.28900578C>GCA2732138548ATP2A1c.1765-3C>G (n.1765-3C>G)
c.1390-3C>G (n.1390-3C>G)
c.794-3C>G
 dbSNP
16g.28900578C>TCA2503425678ATP2A1c.1765-3C>T (n.1765-3C>T)
c.1390-3C>T (n.1390-3C>T)
c.794-3C>T
16g.28900579A>CCA395410828ATP2A1c.1765-2A>C (n.1765-2A>C)
c.1390-2A>C (n.1390-2A>C)
c.794-2A>C
16g.28900579A>GCA395410829ATP2A1c.1765-2A>G (n.1765-2A>G)
c.1390-2A>G (n.1390-2A>G)
c.794-2A>G
 gnomAD v4
16g.28900579A>TCA395410830ATP2A1c.1765-2A>T (n.1765-2A>T)
c.1390-2A>T (n.1390-2A>T)
c.794-2A>T
16g.28900580G>ACA395410832ATP2A1c.1765-1G>A (n.1765-1G>A)
c.1390-1G>A (n.1390-1G>A)
c.794-1G>A
16g.28900580G>CCA395410834ATP2A1c.1765-1G>C (n.1765-1G>C)
c.1390-1G>C (n.1390-1G>C)
c.794-1G>C
16g.28900580G>TCA395410835ATP2A1c.1765-1G>T (n.1765-1G>T)
c.1390-1G>T (n.1390-1G>T)
c.794-1G>T
16g.28900581A=CA2215884251ATP2A1c.1765A= (p.Thr589=)
c.1390A= (p.Thr464=)
c.794A=
16g.28900581A>CCA395410837ATP2A1c.1765A>C (p.Thr589Pro)
c.1390A>C (p.Thr464Pro)
c.794A>C
16g.28900581A>GCA7987079ATP2A1c.1765A>G (p.Thr589Ala)
c.1390A>G (p.Thr464Ala)
c.794A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900581A>TCA395410838ATP2A1c.1765A>T (p.Thr589Ser)
c.1390A>T (p.Thr464Ser)
c.794A>T
16g.28900582C>ACA395410839ATP2A1c.1766C>A (p.Thr589Lys)
c.1391C>A (p.Thr464Lys)
c.795C>A
16g.28900582C=CA2215884260ATP2A1c.1766C= (p.Thr589=)
c.1391C= (p.Thr464=)
c.795C=
16g.28900582C>GCA395410841ATP2A1c.1766C>G (p.Thr589Arg)
c.1391C>G (p.Thr464Arg)
c.795C>G
16g.28900582C>TCA7987080ATP2A1c.1766C>T (p.Thr589Met)
c.1391C>T (p.Thr464Met)
c.795C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900583G>ACA7987081ATP2A1c.1767G>A (p.Thr589=)
c.1392G>A (p.Thr464=)
c.796G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900583G>CCA494508837ATP2A1c.1767G>C (p.Thr589=)
c.1392G>C (p.Thr464=)
c.796G>C
16g.28900583G=CA2215884333ATP2A1c.1767G= (p.Thr589=)
c.1392G= (p.Thr464=)
c.796G=
16g.28900583G>TCA494508834ATP2A1c.1767G>T (p.Thr589=)
c.1392G>T (p.Thr464=)
c.796G>T
16g.28900583_28900584delinsAACA645573194ATP2A1c.1767_1768delinsAA (p.Asp590Asn)
c.1392_1393delinsAA (p.Asp465Asn)
c.796_797delinsAA
 COSMIC
16g.28900584G>ACA279239993ATP2A1c.1768G>A (p.Asp590Asn)
c.1393G>A (p.Asp465Asn)
c.797G>A
 dbSNP gnomAD v2 gnomAD v4
16g.28900584G>CCA395410843ATP2A1c.1768G>C (p.Asp590His)
c.1393G>C (p.Asp465His)
c.797G>C
 gnomAD v4
16g.28900584G=CA2215884351ATP2A1c.1768G= (p.Asp590=)
c.1393G= (p.Asp465=)
c.797G=
16g.28900584G>TCA395410845ATP2A1c.1768G>T (p.Asp590Tyr)
c.1393G>T (p.Asp465Tyr)
c.797G>T
16g.28900585A>CCA395410847ATP2A1c.1769A>C (p.Asp590Ala)
c.1394A>C (p.Asp465Ala)
c.798A>C
16g.28900585A>GCA395410849ATP2A1c.1769A>G (p.Asp590Gly)
c.1394A>G (p.Asp465Gly)
c.798A>G
16g.28900585A>TCA395410851ATP2A1c.1769A>T (p.Asp590Val)
c.1394A>T (p.Asp465Val)
c.798A>T
16g.28900586C>ACA395410853ATP2A1c.1770C>A (p.Asp590Glu)
c.1395C>A (p.Asp465Glu)
c.799C>A
 gnomAD v4
16g.28900586C>GCA395410854ATP2A1c.1770C>G (p.Asp590Glu)
c.1395C>G (p.Asp465Glu)
c.799C>G
16g.28900586C>TCA494508852ATP2A1c.1770C>T (p.Asp590=)
c.1395C>T (p.Asp465=)
c.799C>T
 gnomAD v4
16g.28900587C>ACA395410858ATP2A1c.1771C>A (p.Leu591Met)
c.1396C>A (p.Leu466Met)
c.800C>A
16g.28900587C>GCA395410857ATP2A1c.1771C>G (p.Leu591Val)
c.1396C>G (p.Leu466Val)
c.800C>G
16g.28900587C>TCA494508857ATP2A1c.1771C>T (p.Leu591=)
c.1396C>T (p.Leu466=)
c.800C>T
 dbSNP gnomAD v4
16g.28900588T>ACA395410860ATP2A1c.1772T>A (p.Leu591Gln)
c.1397T>A (p.Leu466Gln)
c.801T>A
16g.28900588T>CCA395410861ATP2A1c.1772T>C (p.Leu591Pro)
c.1397T>C (p.Leu466Pro)
c.801T>C
 gnomAD v4
16g.28900588T>GCA395410862ATP2A1c.1772T>G (p.Leu591Arg)
c.1397T>G (p.Leu466Arg)
c.801T>G
16g.28900589G>ACA279240004ATP2A1c.1773G>A (p.Leu591=)
c.1398G>A (p.Leu466=)
c.802G>A
 dbSNP gnomAD v4
16g.28900589G>CCA494508861ATP2A1c.1773G>C (p.Leu591=)
c.1398G>C (p.Leu466=)
c.802G>C
 gnomAD v4
16g.28900589G=CA2215884358ATP2A1c.1773G= (p.Leu591=)
c.1398G= (p.Leu466=)
c.802G=
16g.28900589G>TCA494508863ATP2A1c.1773G>T (p.Leu591=)
c.1398G>T (p.Leu466=)
c.802G>T
16g.28900590A>CCA395410863ATP2A1c.1774A>C (p.Thr592Pro)
c.1399A>C (p.Thr467Pro)
c.803A>C
16g.28900590A>GCA395410864ATP2A1c.1774A>G (p.Thr592Ala)
c.1399A>G (p.Thr467Ala)
c.803A>G
16g.28900590A>TCA395410865ATP2A1c.1774A>T (p.Thr592Ser)
c.1399A>T (p.Thr467Ser)
c.803A>T
16g.28900591C>ACA395410867ATP2A1c.1775C>A (p.Thr592Lys)
c.1400C>A (p.Thr467Lys)
c.804C>A
 gnomAD v4
16g.28900591C=CA2215884361ATP2A1c.1775C= (p.Thr592=)
c.1400C= (p.Thr467=)
c.804C=
16g.28900591C>GCA395410869ATP2A1c.1775C>G (p.Thr592Arg)
c.1400C>G (p.Thr467Arg)
c.804C>G
 dbSNP gnomAD v4
16g.28900591C>TCA395410870ATP2A1c.1775C>T (p.Thr592Ile)
c.1400C>T (p.Thr467Ile)
c.804C>T
16g.28900592A=CA2215884368ATP2A1c.1776A= (p.Thr592=)
c.1401A= (p.Thr467=)
c.805A=
16g.28900592A>CCA494508884ATP2A1c.1776A>C (p.Thr592=)
c.1401A>C (p.Thr467=)
c.805A>C
 gnomAD v4
16g.28900592A>GCA7987082ATP2A1c.1776A>G (p.Thr592=)
c.1401A>G (p.Thr467=)
c.805A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900592A>TCA494508888ATP2A1c.1776A>T (p.Thr592=)
c.1401A>T (p.Thr467=)
c.805A>T
16g.28900593T>ACA395410874ATP2A1c.1777T>A (p.Phe593Ile)
c.1402T>A (p.Phe468Ile)
c.806T>A
16g.28900593T>CCA395410875ATP2A1c.1777T>C (p.Phe593Leu)
c.1402T>C (p.Phe468Leu)
c.806T>C
 gnomAD v4
16g.28900593T>GCA395410877ATP2A1c.1777T>G (p.Phe593Val)
c.1402T>G (p.Phe468Val)
c.806T>G
16g.28900594T>ACA395410881ATP2A1c.1778T>A (p.Phe593Tyr)
c.1403T>A (p.Phe468Tyr)
c.807T>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900594T>CCA395410883ATP2A1c.1778T>C (p.Phe593Ser)
c.1403T>C (p.Phe468Ser)
c.807T>C
 dbSNP
16g.28900594T>GCA395410880ATP2A1c.1778T>G (p.Phe593Cys)
c.1403T>G (p.Phe468Cys)
c.807T>G
16g.28900594T=CA2215884373ATP2A1c.1778T= (p.Phe593=)
c.1403T= (p.Phe468=)
c.807T=
16g.28900595C>ACA7987083ATP2A1c.1779C>A (p.Phe593Leu)
c.1404C>A (p.Phe468Leu)
c.808C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900595C=CA2215884384ATP2A1c.1779C= (p.Phe593=)
c.1404C= (p.Phe468=)
c.808C=
16g.28900595C>GCA395410885ATP2A1c.1779C>G (p.Phe593Leu)
c.1404C>G (p.Phe468Leu)
c.808C>G
16g.28900595C>TCA7987084ATP2A1c.1779C>T (p.Phe593=)
c.1404C>T (p.Phe468=)
c.808C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900596G>ACA7987085ATP2A1c.1780G>A (p.Val594Met)
c.1405G>A (p.Val469Met)
c.809G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900596G>CCA395410897ATP2A1c.1780G>C (p.Val594Leu)
c.1405G>C (p.Val469Leu)
c.809G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.28900596G=CA2215884392ATP2A1c.1780G= (p.Val594=)
c.1405G= (p.Val469=)
c.809G=
16g.28900596G>TCA395410895ATP2A1c.1780G>T (p.Val594Leu)
c.1405G>T (p.Val469Leu)
c.809G>T
 gnomAD v4 COSMIC
16g.28900597T>ACA395410900ATP2A1c.1781T>A (p.Val594Glu)
c.1406T>A (p.Val469Glu)
c.810T>A
16g.28900597T>CCA395410904ATP2A1c.1781T>C (p.Val594Ala)
c.1406T>C (p.Val469Ala)
c.810T>C
16g.28900597T>GCA395410903ATP2A1c.1781T>G (p.Val594Gly)
c.1406T>G (p.Val469Gly)
c.810T>G
16g.28900598G>ACA494508926ATP2A1c.1782G>A (p.Val594=)
c.1407G>A (p.Val469=)
c.811G>A
 dbSNP gnomAD v4
16g.28900598G>CCA494508925ATP2A1c.1782G>C (p.Val594=)
c.1407G>C (p.Val469=)
c.811G>C
16g.28900598G=CA2215884401ATP2A1c.1782G= (p.Val594=)
c.1407G= (p.Val469=)
c.811G=
16g.28900598G>TCA494508924ATP2A1c.1782G>T (p.Val594=)
c.1407G>T (p.Val469=)
c.811G>T
 dbSNP
16g.28900599G>ACA395410906ATP2A1c.1783G>A (p.Gly595Ser)
c.1408G>A (p.Gly470Ser)
c.812G>A
16g.28900599G>CCA395410908ATP2A1c.1783G>C (p.Gly595Arg)
c.1408G>C (p.Gly470Arg)
c.812G>C
16g.28900599G>TCA395410909ATP2A1c.1783G>T (p.Gly595Cys)
c.1408G>T (p.Gly470Cys)
c.812G>T
 gnomAD v4
16g.28900600G>ACA395410911ATP2A1c.1784G>A (p.Gly595Asp)
c.1409G>A (p.Gly470Asp)
c.813G>A
16g.28900600G>CCA395410913ATP2A1c.1784G>C (p.Gly595Ala)
c.1409G>C (p.Gly470Ala)
c.813G>C
16g.28900600G>TCA395410915ATP2A1c.1784G>T (p.Gly595Val)
c.1409G>T (p.Gly470Val)
c.813G>T
16g.28900601T>ACA494508936ATP2A1c.1785T>A (p.Gly595=)
c.1410T>A (p.Gly470=)
c.814T>A
 gnomAD v4
16g.28900601T>CCA494508939ATP2A1c.1785T>C (p.Gly595=)
c.1410T>C (p.Gly470=)
c.814T>C
 dbSNP gnomAD v4
16g.28900601T>GCA494508941ATP2A1c.1785T>G (p.Gly595=)
c.1410T>G (p.Gly470=)
c.814T>G
16g.28900601_28900602insCTACCA2806424056ATP2A1c.1785_1786insCTAC (p.Val596LeufsTer22)
c.1410_1411insCTAC (p.Val471LeufsTer22)
c.814_815insCTAC
16g.28900602G>ACA7987086ATP2A1c.1786G>A (p.Val596Ile)
c.1411G>A (p.Val471Ile)
c.815G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900602G>CCA395410917ATP2A1c.1786G>C (p.Val596Leu)
c.1411G>C (p.Val471Leu)
c.815G>C
16g.28900602G=CA2215884406ATP2A1c.1786G= (p.Val596=)
c.1411G= (p.Val471=)
c.815G=
16g.28900602G>TCA395410921ATP2A1c.1786G>T (p.Val596Leu)
c.1411G>T (p.Val471Leu)
c.815G>T
16g.28900603T>ACA395410923ATP2A1c.1787T>A (p.Val596Glu)
c.1412T>A (p.Val471Glu)
c.816T>A
16g.28900603T>CCA395410926ATP2A1c.1787T>C (p.Val596Ala)
c.1412T>C (p.Val471Ala)
c.816T>C
 gnomAD v4
16g.28900603T>GCA395410928ATP2A1c.1787T>G (p.Val596Gly)
c.1412T>G (p.Val471Gly)
c.816T>G
16g.28900604A>CCA494874293ATP2A1c.1788A>C (p.Val596=)
c.1413A>C (p.Val471=)
c.817A>C
16g.28900604A>GCA494874294ATP2A1c.1788A>G (p.Val596=)
c.1413A>G (p.Val471=)
c.817A>G
 COSMIC
16g.28900604A>TCA494874295ATP2A1c.1788A>T (p.Val596=)
c.1413A>T (p.Val471=)
c.817A>T
16g.28900605G>ACA395410930ATP2A1c.1789G>A (p.Val597Met)
c.1414G>A (p.Val472Met)
c.818G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900605G>CCA395410934ATP2A1c.1789G>C (p.Val597Leu)
c.1414G>C (p.Val472Leu)
c.818G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900605G=CA2215884414ATP2A1c.1789G= (p.Val597=)
c.1414G= (p.Val472=)
c.818G=
16g.28900605G>TCA395410932ATP2A1c.1789G>T (p.Val597Leu)
c.1414G>T (p.Val472Leu)
c.818G>T
16g.28900606T>ACA395410936ATP2A1c.1790T>A (p.Val597Glu)
c.1415T>A (p.Val472Glu)
c.819T>A
16g.28900606T>CCA395410939ATP2A1c.1790T>C (p.Val597Ala)
c.1415T>C (p.Val472Ala)
c.819T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.28900606T>GCA395410940ATP2A1c.1790T>G (p.Val597Gly)
c.1415T>G (p.Val472Gly)
c.819T>G
16g.28900606T=CA2215884420ATP2A1c.1790T= (p.Val597=)
c.1415T= (p.Val472=)
c.819T=
16g.28900607G>ACA494874296ATP2A1c.1791G>A (p.Val597=)
c.1416G>A (p.Val472=)
c.820G>A
16g.28900607G>CCA494874297ATP2A1c.1791G>C (p.Val597=)
c.1416G>C (p.Val472=)
c.820G>C
16g.28900607G>TCA494874298ATP2A1c.1791G>T (p.Val597=)
c.1416G>T (p.Val472=)
c.820G>T
 gnomAD v4
16g.28900608G>ACA395410943ATP2A1c.1792G>A (p.Gly598Ser)
c.1417G>A (p.Gly473Ser)
c.821G>A
 dbSNP gnomAD v3 gnomAD v4
16g.28900608G>CCA395410944ATP2A1c.1792G>C (p.Gly598Arg)
c.1417G>C (p.Gly473Arg)
c.821G>C
16g.28900608G=CA2215884428ATP2A1c.1792G= (p.Gly598=)
c.1417G= (p.Gly473=)
c.821G=
16g.28900608G>TCA395410945ATP2A1c.1792G>T (p.Gly598Cys)
c.1417G>T (p.Gly473Cys)
c.821G>T
 COSMIC COSMIC
16g.28900609G>ACA395410947ATP2A1c.1793G>A (p.Gly598Asp)
c.1418G>A (p.Gly473Asp)
c.822G>A
 gnomAD v4
16g.28900609G>CCA395410949ATP2A1c.1793G>C (p.Gly598Ala)
c.1418G>C (p.Gly473Ala)
c.822G>C
16g.28900609G>TCA395410951ATP2A1c.1793G>T (p.Gly598Val)
c.1418G>T (p.Gly473Val)
c.822G>T
 gnomAD v4
16g.28900610C>ACA494874299ATP2A1c.1794C>A (p.Gly598=)
c.1419C>A (p.Gly473=)
c.823C>A
16g.28900610C>GCA494874300ATP2A1c.1794C>G (p.Gly598=)
c.1419C>G (p.Gly473=)
c.823C>G
16g.28900610C>TCA494874301ATP2A1c.1794C>T (p.Gly598=)
c.1419C>T (p.Gly473=)
c.823C>T
16g.28900611A>CCA395410954ATP2A1c.1795A>C (p.Met599Leu)
c.1420A>C (p.Met474Leu)
c.824A>C
 gnomAD v4
16g.28900611A>GCA395410955ATP2A1c.1795A>G (p.Met599Val)
c.1420A>G (p.Met474Val)
c.824A>G
16g.28900611A>TCA395410953ATP2A1c.1795A>T (p.Met599Leu)
c.1420A>T (p.Met474Leu)
c.824A>T
16g.28900612T>ACA395410956ATP2A1c.1796T>A (p.Met599Lys)
c.1421T>A (p.Met474Lys)
c.825T>A
16g.28900612T>CCA395410958ATP2A1c.1796T>C (p.Met599Thr)
c.1421T>C (p.Met474Thr)
c.825T>C
 gnomAD v4
16g.28900612T>GCA395410960ATP2A1c.1796T>G (p.Met599Arg)
c.1421T>G (p.Met474Arg)
c.825T>G
16g.28900613G>ACA395410962ATP2A1c.1797G>A (p.Met599Ile)
c.1422G>A (p.Met474Ile)
c.826G>A
16g.28900613G>CCA395410963ATP2A1c.1797G>C (p.Met599Ile)
c.1422G>C (p.Met474Ile)
c.826G>C
16g.28900613G>TCA395410965ATP2A1c.1797G>T (p.Met599Ile)
c.1422G>T (p.Met474Ile)
c.826G>T
 dbSNP
16g.28900615_28900626delCA2575960520ATP2A1c.1799_1810del (p.Leu600_Pro603del)
c.1424_1435del (p.Leu475_Pro478del)
16g.28900614C>ACA395410968ATP2A1c.1798C>A (p.Leu600Met)
c.1423C>A (p.Leu475Met)
c.827C>A
 dbSNP
16g.28900614C>GCA395410969ATP2A1c.1798C>G (p.Leu600Val)
c.1423C>G (p.Leu475Val)
c.827C>G
16g.28900614C>TCA494874302ATP2A1c.1798C>T (p.Leu600=)
c.1423C>T (p.Leu475=)
c.827C>T
 gnomAD v4
16g.28900615T>ACA395410971ATP2A1c.1799T>A (p.Leu600Gln)
c.1424T>A (p.Leu475Gln)
c.828T>A
16g.28900615T>CCA395410974ATP2A1c.1799T>C (p.Leu600Pro)
c.1424T>C (p.Leu475Pro)
c.828T>C
 gnomAD v4
16g.28900615T>GCA395410975ATP2A1c.1799T>G (p.Leu600Arg)
c.1424T>G (p.Leu475Arg)
c.828T>G
16g.28900616G>ACA7987087ATP2A1c.1800G>A (p.Leu600=)
c.1425G>A (p.Leu475=)
c.829G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900616G>CCA494874303ATP2A1c.1800G>C (p.Leu600=)
c.1425G>C (p.Leu475=)
c.829G>C
16g.28900616G=CA2215884439ATP2A1c.1800G= (p.Leu600=)
c.1425G= (p.Leu475=)
c.829G=
16g.28900616G>TCA7987088ATP2A1c.1800G>T (p.Leu600=)
c.1425G>T (p.Leu475=)
c.829G>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900617G>ACA395410983ATP2A1c.1801G>A (p.Asp601Asn)
c.1426G>A (p.Asp476Asn)
c.830G>A
 dbSNP gnomAD v2
16g.28900617G>CCA395410982ATP2A1c.1801G>C (p.Asp601His)
c.1426G>C (p.Asp476His)
c.830G>C
16g.28900617G=CA2215884456ATP2A1c.1801G= (p.Asp601=)
c.1426G= (p.Asp476=)
c.830G=
16g.28900617G>TCA395410981ATP2A1c.1801G>T (p.Asp601Tyr)
c.1426G>T (p.Asp476Tyr)
c.830G>T
16g.28900618A>CCA395410984ATP2A1c.1802A>C (p.Asp601Ala)
c.1427A>C (p.Asp476Ala)
c.831A>C
16g.28900618A>GCA395410985ATP2A1c.1802A>G (p.Asp601Gly)
c.1427A>G (p.Asp476Gly)
c.831A>G
 gnomAD v4
16g.28900618A>TCA395410986ATP2A1c.1802A>T (p.Asp601Val)
c.1427A>T (p.Asp476Val)
c.831A>T
16g.28900619C>ACA395410987ATP2A1c.1803C>A (p.Asp601Glu)
c.1428C>A (p.Asp476Glu)
16g.28900619C=CA2215884463ATP2A1c.1803C= (p.Asp601=)
c.1428C= (p.Asp476=)
16g.28900619C>GCA395410988ATP2A1c.1803C>G (p.Asp601Glu)
c.1428C>G (p.Asp476Glu)
16g.28900619C>TCA7987089ATP2A1c.1803C>T (p.Asp601=)
c.1428C>T (p.Asp476=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900620C>ACA395410989ATP2A1c.1804C>A (p.Pro602Thr)
c.1429C>A (p.Pro477Thr)
 gnomAD v4 COSMIC
16g.28900620C>GCA395410990ATP2A1c.1804C>G (p.Pro602Ala)
c.1429C>G (p.Pro477Ala)
16g.28900620C>TCA395410991ATP2A1c.1804C>T (p.Pro602Ser)
c.1429C>T (p.Pro477Ser)
16g.28900621C>ACA395410992ATP2A1c.1805C>A (p.Pro602His)
c.1430C>A (p.Pro477His)
16g.28900621C=CA2215884465ATP2A1c.1805C= (p.Pro602=)
c.1430C= (p.Pro477=)
16g.28900621C>GCA395410993ATP2A1c.1805C>G (p.Pro602Arg)
c.1430C>G (p.Pro477Arg)
16g.28900621C>TCA395410994ATP2A1c.1805C>T (p.Pro602Leu)
c.1430C>T (p.Pro477Leu)
 dbSNP
16g.28900621_28900622insCGCA2632539884ATP2A1c.1805_1806insCG (p.Pro603ValfsTer20)
c.1430_1431insCG (p.Pro478ValfsTer20)
 gnomAD v4
16g.28900622T>ACA494874304ATP2A1c.1806T>A (p.Pro602=)
c.1431T>A (p.Pro477=)
 dbSNP
16g.28900622T>CCA494874305ATP2A1c.1806T>C (p.Pro602=)
c.1431T>C (p.Pro477=)
16g.28900622T>GCA494874306ATP2A1c.1806T>G (p.Pro602=)
c.1431T>G (p.Pro477=)
16g.28900622T=CA2215884470ATP2A1c.1806T= (p.Pro602=)
c.1431T= (p.Pro477=)
16g.28900622_28900623insACCTTCCCTGCAGACTCACTTCATGCAGTGCACA2632539887ATP2A1c.1806_1807insACCTTCCCTGCAGACTCACTTCATGCAGTGCA (p.Pro603ThrfsTer30)
c.1431_1432insACCTTCCCTGCAGACTCACTTCATGCAGTGCA (p.Pro478ThrfsTer30)
 gnomAD v4
16g.28900623C>ACA395410997ATP2A1c.1807C>A (p.Pro603Thr)
c.1432C>A (p.Pro478Thr)
16g.28900623C>GCA395410996ATP2A1c.1807C>G (p.Pro603Ala)
c.1432C>G (p.Pro478Ala)
16g.28900623C>TCA395410995ATP2A1c.1807C>T (p.Pro603Ser)
c.1432C>T (p.Pro478Ser)
16g.28900624dupCA2215884472ATP2A1c.1808dup (p.Arg604AlafsTer13)
c.1433dup (p.Arg479AlafsTer13)
 dbSNP
16g.28900624C>ACA395410998ATP2A1c.1808C>A (p.Pro603Gln)
c.1433C>A (p.Pro478Gln)
16g.28900624C=CA2215884476ATP2A1c.1808C= (p.Pro603=)
c.1433C= (p.Pro478=)
16g.28900624C>GCA395410999ATP2A1c.1808C>G (p.Pro603Arg)
c.1433C>G (p.Pro478Arg)
 dbSNP gnomAD v2 gnomAD v4
16g.28900624C>TCA7987090ATP2A1c.1808C>T (p.Pro603Leu)
c.1433C>T (p.Pro478Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900625G>ACA7987091ATP2A1c.1809G>A (p.Pro603=)
c.1434G>A (p.Pro478=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900625G>CCA494874308ATP2A1c.1809G>C (p.Pro603=)
c.1434G>C (p.Pro478=)
 dbSNP
16g.28900625G=CA2215884483ATP2A1c.1809G= (p.Pro603=)
c.1434G= (p.Pro478=)
16g.28900625G>TCA494874307ATP2A1c.1809G>T (p.Pro603=)
c.1434G>T (p.Pro478=)
16g.28900626C>ACA395411000ATP2A1c.1810C>A (p.Arg604Ser)
c.1435C>A (p.Arg479Ser)
 gnomAD v4
16g.28900626C=CA2215884492ATP2A1c.1810C= (p.Arg604=)
c.1435C= (p.Arg479=)
16g.28900626C>GCA395411001ATP2A1c.1810C>G (p.Arg604Gly)
c.1435C>G (p.Arg479Gly)
16g.28900626C>TCA279240136ATP2A1c.1810C>T (p.Arg604Cys)
c.1435C>T (p.Arg479Cys)
 ClinVar dbSNP gnomAD v4 COSMIC
16g.28900627G>ACA395411002ATP2A1c.1811G>A (p.Arg604His)
c.1436G>A (p.Arg479His)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.28900627G>CCA395411003ATP2A1c.1811G>C (p.Arg604Pro)
c.1436G>C (p.Arg479Pro)
16g.28900627G=CA2215884501ATP2A1c.1811G= (p.Arg604=)
c.1436G= (p.Arg479=)
16g.28900627G>TCA395411004ATP2A1c.1811G>T (p.Arg604Leu)
c.1436G>T (p.Arg479Leu)
16g.28900628C>ACA494874311ATP2A1c.1812C>A (p.Arg604=)
c.1437C>A (p.Arg479=)
16g.28900628C>GCA494874310ATP2A1c.1812C>G (p.Arg604=)
c.1437C>G (p.Arg479=)
16g.28900628C>TCA494874309ATP2A1c.1812C>T (p.Arg604=)
c.1437C>T (p.Arg479=)
16g.28900629A=CA2215884513ATP2A1c.1813A= (p.Lys605=)
c.1438A= (p.Lys480=)
16g.28900629A>CCA395411005ATP2A1c.1813A>C (p.Lys605Gln)
c.1438A>C (p.Lys480Gln)
16g.28900629A>GCA395411006ATP2A1c.1813A>G (p.Lys605Glu)
c.1438A>G (p.Lys480Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.28900629A>TCA395411007ATP2A1c.1813A>T (p.Lys605Ter)
c.1438A>T (p.Lys480Ter)
16g.28900629_28900632delinsAAGGCA2215884514ATP2A1c.1813_1816delinsAAGG (p.Lys605=)
c.1438_1441delinsAAGG (p.Lys480=)
16g.28900630A>CCA395411008ATP2A1c.1814A>C (p.Lys605Thr)
c.1439A>C (p.Lys480Thr)
16g.28900630A>GCA395411009ATP2A1c.1814A>G (p.Lys605Arg)
c.1439A>G (p.Lys480Arg)
 gnomAD v4
16g.28900630A>TCA395411010ATP2A1c.1814A>T (p.Lys605Met)
c.1439A>T (p.Lys480Met)
16g.28900633_28900635delCA719740017ATP2A1c.1817_1819del (p.Glu606del)
c.1442_1444del (p.Glu481del)
 ClinVar dbSNP
16g.28900631G>ACA494874312ATP2A1c.1815G>A (p.Lys605=)
c.1440G>A (p.Lys480=)
 dbSNP gnomAD v3 gnomAD v4
16g.28900631G>CCA16607383ATP2A1c.1815G>C (p.Lys605Asn)
c.1440G>C (p.Lys480Asn)
 ClinVar dbSNP gnomAD v4
16g.28900631G=CA2215884522ATP2A1c.1815G= (p.Lys605=)
c.1440G= (p.Lys480=)
16g.28900631G>TCA395411011ATP2A1c.1815G>T (p.Lys605Asn)
c.1440G>T (p.Lys480Asn)
 dbSNP
16g.28900632G>ACA395411012ATP2A1c.1816G>A (p.Glu606Lys)
c.1441G>A (p.Glu481Lys)
16g.28900632G>CCA395411013ATP2A1c.1816G>C (p.Glu606Gln)
c.1441G>C (p.Glu481Gln)
16g.28900632G>TCA395411014ATP2A1c.1816G>T (p.Glu606Ter)
c.1441G>T (p.Glu481Ter)
16g.28900633A=CA2215884528ATP2A1c.1817A= (p.Glu606=)
c.1442A= (p.Glu481=)
16g.28900633A>CCA395411015ATP2A1c.1817A>C (p.Glu606Ala)
c.1442A>C (p.Glu481Ala)
16g.28900633A>GCA395411016ATP2A1c.1817A>G (p.Glu606Gly)
c.1442A>G (p.Glu481Gly)
16g.28900633A>TCA7987092ATP2A1c.1817A>T (p.Glu606Val)
c.1442A>T (p.Glu481Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900633_28900634delinsTCCA2580091434ATP2A1c.1817_1818delinsTC (p.Glu606Val)
c.1442_1443delinsTC (p.Glu481Val)
 ClinVar
16g.28900634G>ACA494874313ATP2A1c.1818G>A (p.Glu606=)
c.1443G>A (p.Glu481=)
16g.28900634G>CCA395411017ATP2A1c.1818G>C (p.Glu606Asp)
c.1443G>C (p.Glu481Asp)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900634G=CA2215884531ATP2A1c.1818G= (p.Glu606=)
c.1443G= (p.Glu481=)
16g.28900634G>TCA395411018ATP2A1c.1818G>T (p.Glu606Asp)
c.1443G>T (p.Glu481Asp)
16g.28900635G>ACA395411019ATP2A1c.1819G>A (p.Val607Ile)
c.1444G>A (p.Val482Ile)
16g.28900635G>CCA395411020ATP2A1c.1819G>C (p.Val607Leu)
c.1444G>C (p.Val482Leu)
16g.28900635G>TCA395411021ATP2A1c.1819G>T (p.Val607Phe)
c.1444G>T (p.Val482Phe)
16g.28900636T>ACA395411024ATP2A1c.1820T>A (p.Val607Asp)
c.1445T>A (p.Val482Asp)
16g.28900636T>CCA395411023ATP2A1c.1820T>C (p.Val607Ala)
c.1445T>C (p.Val482Ala)
 gnomAD v4
16g.28900636T>GCA395411022ATP2A1c.1820T>G (p.Val607Gly)
c.1445T>G (p.Val482Gly)
16g.28900637C>ACA494874314ATP2A1c.1821C>A (p.Val607=)
c.1446C>A (p.Val482=)
16g.28900637C>GCA494874315ATP2A1c.1821C>G (p.Val607=)
c.1446C>G (p.Val482=)
16g.28900637C>TCA494874316ATP2A1c.1821C>T (p.Val607=)
c.1446C>T (p.Val482=)
16g.28900638A=CA2215884535ATP2A1c.1822A= (p.Thr608=)
c.1447A= (p.Thr483=)
16g.28900638A>CCA395411025ATP2A1c.1822A>C (p.Thr608Pro)
c.1447A>C (p.Thr483Pro)
16g.28900638A>GCA395411026ATP2A1c.1822A>G (p.Thr608Ala)
c.1447A>G (p.Thr483Ala)
 dbSNP
16g.28900638A>TCA395411027ATP2A1c.1822A>T (p.Thr608Ser)
c.1447A>T (p.Thr483Ser)
16g.28900639C>ACA395411028ATP2A1c.1823C>A (p.Thr608Lys)
c.1448C>A (p.Thr483Lys)
16g.28900639C=CA2215884541ATP2A1c.1823C= (p.Thr608=)
c.1448C= (p.Thr483=)
16g.28900639C>GCA395411029ATP2A1c.1823C>G (p.Thr608Arg)
c.1448C>G (p.Thr483Arg)
16g.28900639C>TCA7987093ATP2A1c.1823C>T (p.Thr608Met)
c.1448C>T (p.Thr483Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900640G>ACA279240147ATP2A1c.1824G>A (p.Thr608=)
c.1449G>A (p.Thr483=)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
16g.28900640G>CCA7987094ATP2A1c.1824G>C (p.Thr608=)
c.1449G>C (p.Thr483=)
 dbSNP ExAC gnomAD v2
16g.28900640G=CA2215884545ATP2A1c.1824G= (p.Thr608=)
c.1449G= (p.Thr483=)
16g.28900640G>TCA494874317ATP2A1c.1824G>T (p.Thr608=)
c.1449G>T (p.Thr483=)
 gnomAD v4
16g.28900641G>ACA395411030ATP2A1c.1825G>A (p.Gly609Ser)
c.1450G>A (p.Gly484Ser)
16g.28900641G>CCA395411032ATP2A1c.1825G>C (p.Gly609Arg)
c.1450G>C (p.Gly484Arg)
16g.28900641G=CA2215884553ATP2A1c.1825G= (p.Gly609=)
c.1450G= (p.Gly484=)
16g.28900641G>TCA395411031ATP2A1c.1825G>T (p.Gly609Cys)
c.1450G>T (p.Gly484Cys)
 dbSNP
16g.28900642G>ACA395411033ATP2A1c.1826G>A (p.Gly609Asp)
c.1451G>A (p.Gly484Asp)
16g.28900642G>CCA395411034ATP2A1c.1826G>C (p.Gly609Ala)
c.1451G>C (p.Gly484Ala)
16g.28900642G>TCA395411035ATP2A1c.1826G>T (p.Gly609Val)
c.1451G>T (p.Gly484Val)
16g.28900643C>ACA494874318ATP2A1c.1827C>A (p.Gly609=)
c.1452C>A (p.Gly484=)
 gnomAD v4
16g.28900643C=CA2215884558ATP2A1c.1827C= (p.Gly609=)
c.1452C= (p.Gly484=)
16g.28900643C>GCA494874319ATP2A1c.1827C>G (p.Gly609=)
c.1452C>G (p.Gly484=)
16g.28900643C>TCA7987095ATP2A1c.1827C>T (p.Gly609=)
c.1452C>T (p.Gly484=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.28900644T>ACA395411036ATP2A1c.1828T>A (p.Ser610Thr)
c.1453T>A (p.Ser485Thr)
16g.28900644T>CCA395411038ATP2A1c.1828T>C (p.Ser610Pro)
c.1453T>C (p.Ser485Pro)
16g.28900644T>GCA395411037ATP2A1c.1828T>G (p.Ser610Ala)
c.1453T>G (p.Ser485Ala)
16g.28900645C>ACA395411039ATP2A1c.1829C>A (p.Ser610Tyr)
c.1454C>A (p.Ser485Tyr)
16g.28900645C>GCA395411040ATP2A1c.1829C>G (p.Ser610Cys)
c.1454C>G (p.Ser485Cys)
16g.28900645C>TCA395411041ATP2A1c.1829C>T (p.Ser610Phe)
c.1454C>T (p.Ser485Phe)
16g.28900646C>ACA494874320ATP2A1c.1830C>A (p.Ser610=)
c.1455C>A (p.Ser485=)
 gnomAD v4
16g.28900646C=CA2215884562ATP2A1c.1830C= (p.Ser610=)
c.1455C= (p.Ser485=)
16g.28900646C>GCA494874321ATP2A1c.1830C>G (p.Ser610=)
c.1455C>G (p.Ser485=)
16g.28900646C>TCA279240150ATP2A1c.1830C>T (p.Ser610=)
c.1455C>T (p.Ser485=)
 dbSNP
16g.28900647A>CCA395411042ATP2A1c.1831A>C (p.Ile611Leu)
c.1456A>C (p.Ile486Leu)
16g.28900647A>GCA395411043ATP2A1c.1831A>G (p.Ile611Val)
c.1456A>G (p.Ile486Val)
16g.28900647A>TCA395411044ATP2A1c.1831A>T (p.Ile611Phe)
c.1456A>T (p.Ile486Phe)
16g.28900648T>ACA395411045ATP2A1c.1832T>A (p.Ile611Asn)
c.1457T>A (p.Ile486Asn)
16g.28900648T>CCA395411046ATP2A1c.1832T>C (p.Ile611Thr)
c.1457T>C (p.Ile486Thr)
16g.28900648T>GCA395411047ATP2A1c.1832T>G (p.Ile611Ser)
c.1457T>G (p.Ile486Ser)
16g.28900649C>ACA494874322ATP2A1c.1833C>A (p.Ile611=)
c.1458C>A (p.Ile486=)
16g.28900649C>GCA395411048ATP2A1c.1833C>G (p.Ile611Met)
c.1458C>G (p.Ile486Met)
 COSMIC
16g.28900649C>TCA494874323ATP2A1c.1833C>T (p.Ile611=)
c.1458C>T (p.Ile486=)
16g.28900650C>ACA395411051ATP2A1c.1834C>A (p.Gln612Lys)
c.1459C>A (p.Gln487Lys)
16g.28900650C>GCA395411050ATP2A1c.1834C>G (p.Gln612Glu)
c.1459C>G (p.Gln487Glu)
16g.28900650C>TCA395411049ATP2A1c.1834C>T (p.Gln612Ter)
c.1459C>T (p.Gln487Ter)
 gnomAD v4
16g.28900651_28900658dupCA2632539929ATP2A1c.1835_1842dup (p.Arg615SerfsTer10)
c.1460_1467dup (p.Arg490SerfsTer10)
 gnomAD v4
16g.28900651A>CCA395411052ATP2A1c.1835A>C (p.Gln612Pro)
c.1460A>C (p.Gln487Pro)
16g.28900651A>GCA395411054ATP2A1c.1835A>G (p.Gln612Arg)
c.1460A>G (p.Gln487Arg)
16g.28900651A>TCA395411053ATP2A1c.1835A>T (p.Gln612Leu)
c.1460A>T (p.Gln487Leu)
16g.28900652G>ACA494874324ATP2A1c.1836G>A (p.Gln612=)
c.1461G>A (p.Gln487=)
 dbSNP
16g.28900652G>CCA395411055ATP2A1c.1836G>C (p.Gln612His)
c.1461G>C (p.Gln487His)
 dbSNP gnomAD v4
16g.28900652G=CA2215884569ATP2A1c.1836G= (p.Gln612=)
c.1461G= (p.Gln487=)
16g.28900652G>TCA395411056ATP2A1c.1836G>T (p.Gln612His)
c.1461G>T (p.Gln487His)
16g.28900653C>ACA395411057ATP2A1c.1837C>A (p.Leu613Met)
c.1462C>A (p.Leu488Met)
16g.28900653C=CA2215884572ATP2A1c.1837C= (p.Leu613=)
c.1462C= (p.Leu488=)
16g.28900653C>GCA395411058ATP2A1c.1837C>G (p.Leu613Val)
c.1462C>G (p.Leu488Val)
16g.28900653C>TCA7987096ATP2A1c.1837C>T (p.Leu613=)
c.1462C>T (p.Leu488=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900654T>ACA395411059ATP2A1c.1838T>A (p.Leu613Gln)
c.1463T>A (p.Leu488Gln)
16g.28900654T>CCA395411060ATP2A1c.1838T>C (p.Leu613Pro)
c.1463T>C (p.Leu488Pro)
16g.28900654T>GCA395411061ATP2A1c.1838T>G (p.Leu613Arg)
c.1463T>G (p.Leu488Arg)
16g.28900655G>ACA494874325ATP2A1c.1839G>A (p.Leu613=)
c.1464G>A (p.Leu488=)
 dbSNP gnomAD v4
16g.28900655G>CCA494874326ATP2A1c.1839G>C (p.Leu613=)
c.1464G>C (p.Leu488=)
16g.28900655G>TCA494874327ATP2A1c.1839G>T (p.Leu613=)
c.1464G>T (p.Leu488=)
16g.28900656T>ACA395411062ATP2A1c.1840T>A (p.Cys614Ser)
c.1465T>A (p.Cys489Ser)
16g.28900656T>CCA395411063ATP2A1c.1840T>C (p.Cys614Arg)
c.1465T>C (p.Cys489Arg)
 gnomAD v4
16g.28900656T>GCA395411064ATP2A1c.1840T>G (p.Cys614Gly)
c.1465T>G (p.Cys489Gly)
16g.28900657G>ACA395411065ATP2A1c.1841G>A (p.Cys614Tyr)
c.1466G>A (p.Cys489Tyr)
16g.28900657G>CCA395411066ATP2A1c.1841G>C (p.Cys614Ser)
c.1466G>C (p.Cys489Ser)
16g.28900657G>TCA395411067ATP2A1c.1841G>T (p.Cys614Phe)
c.1466G>T (p.Cys489Phe)
16g.28900658C>ACA395411069ATP2A1c.1842C>A (p.Cys614Ter)
c.1467C>A (p.Cys489Ter)
16g.28900658C=CA2215884579ATP2A1c.1842C= (p.Cys614=)
c.1467C= (p.Cys489=)
16g.28900658C>GCA395411068ATP2A1c.1842C>G (p.Cys614Trp)
c.1467C>G (p.Cys489Trp)
16g.28900658C>TCA494874328ATP2A1c.1842C>T (p.Cys614=)
c.1467C>T (p.Cys489=)
 dbSNP gnomAD v2 gnomAD v4
16g.28900659C>ACA395411070ATP2A1c.1843C>A (p.Arg615Ser)
c.1468C>A (p.Arg490Ser)
16g.28900659C=CA2215884587ATP2A1c.1843C= (p.Arg615=)
c.1468C= (p.Arg490=)
16g.28900659C>GCA395411071ATP2A1c.1843C>G (p.Arg615Gly)
c.1468C>G (p.Arg490Gly)
 ClinVar dbSNP gnomAD v4
16g.28900659C>TCA7987097ATP2A1c.1843C>T (p.Arg615Cys)
c.1468C>T (p.Arg490Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900660G>ACA7987098ATP2A1c.1844G>A (p.Arg615His)
c.1469G>A (p.Arg490His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.28900660G>CCA395411072ATP2A1c.1844G>C (p.Arg615Pro)
c.1469G>C (p.Arg490Pro)
 gnomAD v4
16g.28900660G=CA2215884594ATP2A1c.1844G= (p.Arg615=)
c.1469G= (p.Arg490=)
16g.28900660G>TCA395411073ATP2A1c.1844G>T (p.Arg615Leu)
c.1469G>T (p.Arg490Leu)
16g.28900661T>ACA494874329ATP2A1c.1845T>A (p.Arg615=)
c.1470T>A (p.Arg490=)
 dbSNP
16g.28900661T>CCA494874330ATP2A1c.1845T>C (p.Arg615=)
c.1470T>C (p.Arg490=)
16g.28900661T>GCA494874331ATP2A1c.1845T>G (p.Arg615=)
c.1470T>G (p.Arg490=)
16g.28900662G>ACA395411074ATP2A1c.1846G>A (p.Asp616Asn)
c.1471G>A (p.Asp491Asn)
16g.28900662G>CCA395411075ATP2A1c.1846G>C (p.Asp616His)
c.1471G>C (p.Asp491His)
16g.28900662G>TCA395411076ATP2A1c.1846G>T (p.Asp616Tyr)
c.1471G>T (p.Asp491Tyr)
16g.28900663A>CCA395411077ATP2A1c.1847A>C (p.Asp616Ala)
c.1472A>C (p.Asp491Ala)
16g.28900663A>GCA395411078ATP2A1c.1847A>G (p.Asp616Gly)
c.1472A>G (p.Asp491Gly)
 gnomAD v4
16g.28900663A>TCA395411079ATP2A1c.1847A>T (p.Asp616Val)
c.1472A>T (p.Asp491Val)
 COSMIC COSMIC
16g.28900664C>ACA395411081ATP2A1c.1848C>A (p.Asp616Glu)
c.1473C>A (p.Asp491Glu)
16g.28900664C=CA2215884598ATP2A1c.1848C= (p.Asp616=)
c.1473C= (p.Asp491=)
16g.28900664C>GCA395411080ATP2A1c.1848C>G (p.Asp616Glu)
c.1473C>G (p.Asp491Glu)
16g.28900664C>TCA7987099ATP2A1c.1848C>T (p.Asp616=)
c.1473C>T (p.Asp491=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched