Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.138732959delCA2579035692ATP6V0A4c.1830del (p.Ser611AlafsTer?)
c.1056del (p.Ser353AlafsTer?)
c.723del (p.Ser242AlafsTer?)
7g.138732956G>ACA369379024ATP6V0A4c.1829C>T (p.Pro610Leu)
c.1055C>T (p.Pro352Leu)
c.722C>T (p.Pro241Leu)
7g.138732956G>CCA369379026ATP6V0A4c.1829C>G (p.Pro610Arg)
c.1055C>G (p.Pro352Arg)
c.722C>G (p.Pro241Arg)
7g.138732956G>TCA369379029ATP6V0A4c.1829C>A (p.Pro610His)
c.1055C>A (p.Pro352His)
c.722C>A (p.Pro241His)
7g.138732957G>ACA369379036ATP6V0A4c.1828C>T (p.Pro610Ser)
c.1054C>T (p.Pro352Ser)
c.721C>T (p.Pro241Ser)
 dbSNP gnomAD v3 gnomAD v4
7g.138732957G>CCA369379035ATP6V0A4c.1828C>G (p.Pro610Ala)
c.1054C>G (p.Pro352Ala)
c.721C>G (p.Pro241Ala)
7g.138732957G=CA1746776850ATP6V0A4c.1828C= (p.Pro610=)
c.1054C= (p.Pro352=)
c.721C= (p.Pro241=)
7g.138732957G>TCA369379033ATP6V0A4c.1828C>A (p.Pro610Thr)
c.1054C>A (p.Pro352Thr)
c.721C>A (p.Pro241Thr)
7g.138732958G>ACA458150220ATP6V0A4c.1827C>T (p.Ala609=)
c.1053C>T (p.Ala351=)
c.720C>T (p.Ala240=)
7g.138732958G>CCA458150222ATP6V0A4c.1827C>G (p.Ala609=)
c.1053C>G (p.Ala351=)
c.720C>G (p.Ala240=)
7g.138732958G>TCA458150221ATP6V0A4c.1827C>A (p.Ala609=)
c.1053C>A (p.Ala351=)
c.720C>A (p.Ala240=)
 gnomAD v4
7g.138732959G>ACA167133066ATP6V0A4c.1826C>T (p.Ala609Val)
c.1052C>T (p.Ala351Val)
c.719C>T (p.Ala240Val)
 dbSNP gnomAD v4
7g.138732959G>CCA369379040ATP6V0A4c.1826C>G (p.Ala609Gly)
c.1052C>G (p.Ala351Gly)
c.719C>G (p.Ala240Gly)
7g.138732959G=CA1746776851ATP6V0A4c.1826C= (p.Ala609=)
c.1052C= (p.Ala351=)
c.719C= (p.Ala240=)
7g.138732959G>TCA369379042ATP6V0A4c.1826C>A (p.Ala609Asp)
c.1052C>A (p.Ala351Asp)
c.719C>A (p.Ala240Asp)
7g.138732960C>ACA369379045ATP6V0A4c.1825G>T (p.Ala609Ser)
c.1051G>T (p.Ala351Ser)
c.718G>T (p.Ala240Ser)
 gnomAD v4
7g.138732960C=CA1746776852ATP6V0A4c.1825G= (p.Ala609=)
c.1051G= (p.Ala351=)
c.718G= (p.Ala240=)
7g.138732960C>GCA369379048ATP6V0A4c.1825G>C (p.Ala609Pro)
c.1051G>C (p.Ala351Pro)
c.718G>C (p.Ala240Pro)
7g.138732960C>TCA4504644ATP6V0A4c.1825G>A (p.Ala609Thr)
c.1051G>A (p.Ala351Thr)
c.718G>A (p.Ala240Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.138732961G>ACA4504645ATP6V0A4c.1824C>T (p.His608=)
c.1050C>T (p.His350=)
c.717C>T (p.His239=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.138732961G>CCA369379054ATP6V0A4c.1824C>G (p.His608Gln)
c.1050C>G (p.His350Gln)
c.717C>G (p.His239Gln)
7g.138732961G=CA1746776853ATP6V0A4c.1824C= (p.His608=)
c.1050C= (p.His350=)
c.717C= (p.His239=)
7g.138732961G>TCA369379055ATP6V0A4c.1824C>A (p.His608Gln)
c.1050C>A (p.His350Gln)
c.717C>A (p.His239Gln)
7g.138732962T>ACA369379059ATP6V0A4c.1823A>T (p.His608Leu)
c.1049A>T (p.His350Leu)
c.716A>T (p.His239Leu)
7g.138732962T>CCA369379061ATP6V0A4c.1823A>G (p.His608Arg)
c.1049A>G (p.His350Arg)
c.716A>G (p.His239Arg)
7g.138732962T>GCA369379066ATP6V0A4c.1823A>C (p.His608Pro)
c.1049A>C (p.His350Pro)
c.716A>C (p.His239Pro)
7g.138732963G>ACA369379069ATP6V0A4c.1822C>T (p.His608Tyr)
c.1048C>T (p.His350Tyr)
c.715C>T (p.His239Tyr)
7g.138732963G>CCA369379071ATP6V0A4c.1822C>G (p.His608Asp)
c.1048C>G (p.His350Asp)
c.715C>G (p.His239Asp)
7g.138732963G>TCA369379068ATP6V0A4c.1822C>A (p.His608Asn)
c.1048C>A (p.His350Asn)
c.715C>A (p.His239Asn)
7g.138732964C>ACA369379074ATP6V0A4c.1821G>T (p.Gln607His)
c.1047G>T (p.Gln349His)
c.714G>T (p.Gln238His)
7g.138732964C>GCA369379077ATP6V0A4c.1821G>C (p.Gln607His)
c.1047G>C (p.Gln349His)
c.714G>C (p.Gln238His)
7g.138732964C>TCA458150223ATP6V0A4c.1821G>A (p.Gln607=)
c.1047G>A (p.Gln349=)
c.714G>A (p.Gln238=)
7g.138732965T>ACA369379080ATP6V0A4c.1820A>T (p.Gln607Leu)
c.1046A>T (p.Gln349Leu)
c.713A>T (p.Gln238Leu)
7g.138732965T>CCA369379083ATP6V0A4c.1820A>G (p.Gln607Arg)
c.1046A>G (p.Gln349Arg)
c.713A>G (p.Gln238Arg)
7g.138732965T>GCA369379085ATP6V0A4c.1820A>C (p.Gln607Pro)
c.1046A>C (p.Gln349Pro)
c.713A>C (p.Gln238Pro)
7g.138732966G>ACA369379092ATP6V0A4c.1819C>T (p.Gln607Ter)
c.1045C>T (p.Gln349Ter)
c.712C>T (p.Gln238Ter)
7g.138732966G>CCA369379090ATP6V0A4c.1819C>G (p.Gln607Glu)
c.1045C>G (p.Gln349Glu)
c.712C>G (p.Gln238Glu)
7g.138732966G>TCA369379088ATP6V0A4c.1819C>A (p.Gln607Lys)
c.1045C>A (p.Gln349Lys)
c.712C>A (p.Gln238Lys)
7g.138732967A>CCA458150224ATP6V0A4c.1818T>G (p.Ser606=)
c.1044T>G (p.Ser348=)
c.711T>G (p.Ser237=)
7g.138732967A>GCA458150225ATP6V0A4c.1818T>C (p.Ser606=)
c.1044T>C (p.Ser348=)
c.711T>C (p.Ser237=)
7g.138732967A>TCA458150226ATP6V0A4c.1818T>A (p.Ser606=)
c.1044T>A (p.Ser348=)
c.711T>A (p.Ser237=)
7g.138732968G>ACA369379095ATP6V0A4c.1817C>T (p.Ser606Phe)
c.1043C>T (p.Ser348Phe)
c.710C>T (p.Ser237Phe)
7g.138732968G>CCA369379097ATP6V0A4c.1817C>G (p.Ser606Cys)
c.1043C>G (p.Ser348Cys)
c.710C>G (p.Ser237Cys)
7g.138732968G>TCA369379098ATP6V0A4c.1817C>A (p.Ser606Tyr)
c.1043C>A (p.Ser348Tyr)
c.710C>A (p.Ser237Tyr)
7g.138732969A>CCA369379101ATP6V0A4c.1816T>G (p.Ser606Ala)
c.1042T>G (p.Ser348Ala)
c.709T>G (p.Ser237Ala)
7g.138732969A>GCA369379103ATP6V0A4c.1816T>C (p.Ser606Pro)
c.1042T>C (p.Ser348Pro)
c.709T>C (p.Ser237Pro)
7g.138732969A>TCA369379106ATP6V0A4c.1816T>A (p.Ser606Thr)
c.1042T>A (p.Ser348Thr)
c.709T>A (p.Ser237Thr)
7g.138732970T>ACA458150227ATP6V0A4c.1815A>T (p.Val605=)
c.1041A>T (p.Val347=)
c.708A>T (p.Val236=)
 gnomAD v4
7g.138732970T>CCA458150228ATP6V0A4c.1815A>G (p.Val605=)
c.1041A>G (p.Val347=)
c.708A>G (p.Val236=)
 dbSNP gnomAD v2
7g.138732970T>GCA458150229ATP6V0A4c.1815A>C (p.Val605=)
c.1041A>C (p.Val347=)
c.708A>C (p.Val236=)

Number of alleles fetched