Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47795896_47805709delCA658655622MSH6c.460_3646+2del
c.238-2715_3256+2del
c.163_3349+2del
c.169+2491_170-6451del (p.=)
c.*124+2290_*125-6451del (p.=)
c.458-2715_*2993+2del
c.-443_2740+2del
c.-279-2715_2740+2del
c.-2637_550+2del
c.277_3463+2del
2g.47799557_47804482dupCA10575504MSH6c.1574_3439-428dup
c.1184_3049-428dup
c.1277_3142-428dup
c.169+3714_169+8639dup (p.=)
c.*124+3513_*124+8438dup (p.=)
c.*921_*2786-428dup
c.668_2533-428dup
c.-1523_335-420dup
c.1391_3256-428dup
ClinVar
2g.47799830C>ACA346749688MSH6c.1847C>A (p.Ser616Tyr)
c.1457C>A (p.Ser486Tyr)
c.1550C>A (p.Ser517Tyr)
c.169+8365G>T (p.=)
c.*124+8164G>T (p.=)
c.*1194C>A (p.=)
c.941C>A (p.Ser314Tyr)
c.1844C>A (p.Ser615Tyr)
c.-1250C>A (p.=)
c.1664C>A (p.Ser555Tyr)
COSMIC
2g.47799830C=CA2496049040MSH6c.1847C= (p.Ser616=)
c.1457C= (p.Ser486=)
c.1550C= (p.Ser517=)
c.169+8365G= (p.=)
c.*124+8164G= (p.=)
c.*1194C= (p.=)
c.941C= (p.Ser314=)
c.1844C= (p.Ser615=)
c.-1250C= (p.=)
c.1664C= (p.Ser555=)
2g.47799830C>GCA068191MSH6c.1847C>G (p.Ser616Cys)
c.1457C>G (p.Ser486Cys)
c.1550C>G (p.Ser517Cys)
c.169+8365G>C (p.=)
c.*124+8164G>C (p.=)
c.*1194C>G (p.=)
c.941C>G (p.Ser314Cys)
c.1844C>G (p.Ser615Cys)
c.-1250C>G (p.=)
c.1664C>G (p.Ser555Cys)
ClinVar dbSNP ExAC gnomAD
2g.47799830C>TCA346749690MSH6c.1847C>T (p.Ser616Phe)
c.1457C>T (p.Ser486Phe)
c.1550C>T (p.Ser517Phe)
c.169+8365G>A (p.=)
c.*124+8164G>A (p.=)
c.*1194C>T (p.=)
c.941C>T (p.Ser314Phe)
c.1844C>T (p.Ser615Phe)
c.-1250C>T (p.=)
c.1664C>T (p.Ser555Phe)
ClinVar gnomAD
2g.47799831T>ACA426121247MSH6c.1848T>A (p.Ser616=)
c.1458T>A (p.Ser486=)
c.1551T>A (p.Ser517=)
c.169+8364A>T (p.=)
c.*124+8163A>T (p.=)
c.*1195T>A (p.=)
c.942T>A (p.Ser314=)
c.1845T>A (p.Ser615=)
c.-1249T>A (p.=)
c.1665T>A (p.Ser555=)
2g.47799831T>CCA426121248MSH6c.1848T>C (p.Ser616=)
c.1458T>C (p.Ser486=)
c.1551T>C (p.Ser517=)
c.169+8364A>G (p.=)
c.*124+8163A>G (p.=)
c.*1195T>C (p.=)
c.942T>C (p.Ser314=)
c.1845T>C (p.Ser615=)
c.-1249T>C (p.=)
c.1665T>C (p.Ser555=)
2g.47799831T>GCA426121249MSH6c.1848T>G (p.Ser616=)
c.1458T>G (p.Ser486=)
c.1551T>G (p.Ser517=)
c.169+8364A>C (p.=)
c.*124+8163A>C (p.=)
c.*1195T>G (p.=)
c.942T>G (p.Ser314=)
c.1845T>G (p.Ser615=)
c.-1249T>G (p.=)
c.1665T>G (p.Ser555=)
2g.47799832C>ACA068196MSH6c.1849C>A (p.Leu617Ile)
c.1459C>A (p.Leu487Ile)
c.1552C>A (p.Leu518Ile)
c.169+8363G>T (p.=)
c.*124+8162G>T (p.=)
c.*1196C>A (p.=)
c.943C>A (p.Leu315Ile)
c.1846C>A (p.Leu616Ile)
c.-1248C>A (p.=)
c.1666C>A (p.Leu556Ile)
ClinVar dbSNP ExAC gnomAD
2g.47799832C=CA2496049041MSH6c.1849C= (p.Leu617=)
c.1459C= (p.Leu487=)
c.1552C= (p.Leu518=)
c.169+8363G= (p.=)
c.*124+8162G= (p.=)
c.*1196C= (p.=)
c.943C= (p.Leu315=)
c.1846C= (p.Leu616=)
c.-1248C= (p.=)
c.1666C= (p.Leu556=)
2g.47799832C>GCA346749702MSH6c.1849C>G (p.Leu617Val)
c.1459C>G (p.Leu487Val)
c.1552C>G (p.Leu518Val)
c.169+8363G>C (p.=)
c.*124+8162G>C (p.=)
c.*1196C>G (p.=)
c.943C>G (p.Leu315Val)
c.1846C>G (p.Leu616Val)
c.-1248C>G (p.=)
c.1666C>G (p.Leu556Val)
2g.47799832C>TCA346749707MSH6c.1849C>T (p.Leu617Phe)
c.1459C>T (p.Leu487Phe)
c.1552C>T (p.Leu518Phe)
c.169+8363G>A (p.=)
c.*124+8162G>A (p.=)
c.*1196C>T (p.=)
c.943C>T (p.Leu315Phe)
c.1846C>T (p.Leu616Phe)
c.-1248C>T (p.=)
c.1666C>T (p.Leu556Phe)
ClinVar
2g.47799833T>ACA346749714MSH6c.1850T>A (p.Leu617His)
c.1460T>A (p.Leu487His)
c.1553T>A (p.Leu518His)
c.169+8362A>T (p.=)
c.*124+8161A>T (p.=)
c.*1197T>A (p.=)
c.944T>A (p.Leu315His)
c.1847T>A (p.Leu616His)
c.-1247T>A (p.=)
c.1667T>A (p.Leu556His)
2g.47799833T>CCA346749730MSH6c.1850T>C (p.Leu617Pro)
c.1460T>C (p.Leu487Pro)
c.1553T>C (p.Leu518Pro)
c.169+8362A>G (p.=)
c.*124+8161A>G (p.=)
c.*1197T>C (p.=)
c.944T>C (p.Leu315Pro)
c.1847T>C (p.Leu616Pro)
c.-1247T>C (p.=)
c.1667T>C (p.Leu556Pro)
2g.47799833T>GCA346749734MSH6c.1850T>G (p.Leu617Arg)
c.1460T>G (p.Leu487Arg)
c.1553T>G (p.Leu518Arg)
c.169+8362A>C (p.=)
c.*124+8161A>C (p.=)
c.*1197T>G (p.=)
c.944T>G (p.Leu315Arg)
c.1847T>G (p.Leu616Arg)
c.-1247T>G (p.=)
c.1667T>G (p.Leu556Arg)
ClinVar
2g.47799833T=CA2496049042MSH6c.1850T= (p.Leu617=)
c.1460T= (p.Leu487=)
c.1553T= (p.Leu518=)
c.169+8362A= (p.=)
c.*124+8161A= (p.=)
c.*1197T= (p.=)
c.944T= (p.Leu315=)
c.1847T= (p.Leu616=)
c.-1247T= (p.=)
c.1667T= (p.Leu556=)
2g.47799834T>ACA426121253MSH6c.1851T>A (p.Leu617=)
c.1461T>A (p.Leu487=)
c.1554T>A (p.Leu518=)
c.169+8361A>T (p.=)
c.*124+8160A>T (p.=)
c.*1198T>A (p.=)
c.945T>A (p.Leu315=)
c.1848T>A (p.Leu616=)
c.-1246T>A (p.=)
c.1668T>A (p.Leu556=)
2g.47799834T>CCA426121254MSH6c.1851T>C (p.Leu617=)
c.1461T>C (p.Leu487=)
c.1554T>C (p.Leu518=)
c.169+8361A>G (p.=)
c.*124+8160A>G (p.=)
c.*1198T>C (p.=)
c.945T>C (p.Leu315=)
c.1848T>C (p.Leu616=)
c.-1246T>C (p.=)
c.1668T>C (p.Leu556=)
COSMIC
2g.47799834T>GCA426121255MSH6c.1851T>G (p.Leu617=)
c.1461T>G (p.Leu487=)
c.1554T>G (p.Leu518=)
c.169+8361A>C (p.=)
c.*124+8160A>C (p.=)
c.*1198T>G (p.=)
c.945T>G (p.Leu315=)
c.1848T>G (p.Leu616=)
c.-1246T>G (p.=)
c.1668T>G (p.Leu556=)
2g.47799835C>ACA346749742MSH6c.1852C>A (p.Gln618Lys)
c.1462C>A (p.Gln488Lys)
c.1555C>A (p.Gln519Lys)
c.169+8360G>T (p.=)
c.*124+8159G>T (p.=)
c.*1199C>A (p.=)
c.946C>A (p.Gln316Lys)
c.1849C>A (p.Gln617Lys)
c.-1245C>A (p.=)
c.1669C>A (p.Gln557Lys)
2g.47799835C=CA2496049043MSH6c.1852C= (p.Gln618=)
c.1462C= (p.Gln488=)
c.1555C= (p.Gln519=)
c.169+8360G= (p.=)
c.*124+8159G= (p.=)
c.*1199C= (p.=)
c.946C= (p.Gln316=)
c.1849C= (p.Gln617=)
c.-1245C= (p.=)
c.1669C= (p.Gln557=)
2g.47799835C>GCA346749737MSH6c.1852C>G (p.Gln618Glu)
c.1462C>G (p.Gln488Glu)
c.1555C>G (p.Gln519Glu)
c.169+8360G>C (p.=)
c.*124+8159G>C (p.=)
c.*1199C>G (p.=)
c.946C>G (p.Gln316Glu)
c.1849C>G (p.Gln617Glu)
c.-1245C>G (p.=)
c.1669C>G (p.Gln557Glu)
gnomAD
2g.47799835C>TCA346749739MSH6c.1852C>T (p.Gln618Ter)
c.1462C>T (p.Gln488Ter)
c.1555C>T (p.Gln519Ter)
c.169+8360G>A (p.=)
c.*124+8159G>A (p.=)
c.*1199C>T (p.=)
c.946C>T (p.Gln316Ter)
c.1849C>T (p.Gln617Ter)
c.-1245C>T (p.=)
c.1669C>T (p.Gln557Ter)
COSMIC
2g.47799836A=CA2496049044MSH6c.1853A= (p.Gln618=)
c.1463A= (p.Gln488=)
c.1556A= (p.Gln519=)
c.169+8359T= (p.=)
c.*124+8158T= (p.=)
c.*1200A= (p.=)
c.947A= (p.Gln316=)
c.1850A= (p.Gln617=)
c.-1244A= (p.=)
c.1670A= (p.Gln557=)
2g.47799836A>CCA346749745MSH6c.1853A>C (p.Gln618Pro)
c.1463A>C (p.Gln488Pro)
c.1556A>C (p.Gln519Pro)
c.169+8359T>G (p.=)
c.*124+8158T>G (p.=)
c.*1200A>C (p.=)
c.947A>C (p.Gln316Pro)
c.1850A>C (p.Gln617Pro)
c.-1244A>C (p.=)
c.1670A>C (p.Gln557Pro)
ClinVar
2g.47799836A>GCA068201MSH6c.1853A>G (p.Gln618Arg)
c.1463A>G (p.Gln488Arg)
c.1556A>G (p.Gln519Arg)
c.169+8359T>C (p.=)
c.*124+8158T>C (p.=)
c.*1200A>G (p.=)
c.947A>G (p.Gln316Arg)
c.1850A>G (p.Gln617Arg)
c.-1244A>G (p.=)
c.1670A>G (p.Gln557Arg)
dbSNP ExAC gnomAD
2g.47799836A>TCA346749752MSH6c.1853A>T (p.Gln618Leu)
c.1463A>T (p.Gln488Leu)
c.1556A>T (p.Gln519Leu)
c.169+8359T>A (p.=)
c.*124+8158T>A (p.=)
c.*1200A>T (p.=)
c.947A>T (p.Gln316Leu)
c.1850A>T (p.Gln617Leu)
c.-1244A>T (p.=)
c.1670A>T (p.Gln557Leu)
2g.47799837G>ACA426121256MSH6c.1854G>A (p.Gln618=)
c.1464G>A (p.Gln488=)
c.1557G>A (p.Gln519=)
c.169+8358C>T (p.=)
c.*124+8157C>T (p.=)
c.*1201G>A (p.=)
c.948G>A (p.Gln316=)
c.1851G>A (p.Gln617=)
c.-1243G>A (p.=)
c.1671G>A (p.Gln557=)
2g.47799837G>CCA346749757MSH6c.1854G>C (p.Gln618His)
c.1464G>C (p.Gln488His)
c.1557G>C (p.Gln519His)
c.169+8358C>G (p.=)
c.*124+8157C>G (p.=)
c.*1201G>C (p.=)
c.948G>C (p.Gln316His)
c.1851G>C (p.Gln617His)
c.-1243G>C (p.=)
c.1671G>C (p.Gln557His)
2g.47799837G>TCA346749760MSH6c.1854G>T (p.Gln618His)
c.1464G>T (p.Gln488His)
c.1557G>T (p.Gln519His)
c.169+8358C>A (p.=)
c.*124+8157C>A (p.=)
c.*1201G>T (p.=)
c.948G>T (p.Gln316His)
c.1851G>T (p.Gln617His)
c.-1243G>T (p.=)
c.1671G>T (p.Gln557His)
2g.47799838G>ACA346749766MSH6c.1855G>A (p.Glu619Lys)
c.1465G>A (p.Glu489Lys)
c.1558G>A (p.Glu520Lys)
c.169+8357C>T (p.=)
c.*124+8156C>T (p.=)
c.*1202G>A (p.=)
c.949G>A (p.Glu317Lys)
c.1852G>A (p.Glu618Lys)
c.-1242G>A (p.=)
c.1672G>A (p.Glu558Lys)
ClinVar
2g.47799838G>CCA346749763MSH6c.1855G>C (p.Glu619Gln)
c.1465G>C (p.Glu489Gln)
c.1558G>C (p.Glu520Gln)
c.169+8357C>G (p.=)
c.*124+8156C>G (p.=)
c.*1202G>C (p.=)
c.949G>C (p.Glu317Gln)
c.1852G>C (p.Glu618Gln)
c.-1242G>C (p.=)
c.1672G>C (p.Glu558Gln)
2g.47799838G=CA2496049045MSH6c.1855G= (p.Glu619=)
c.1465G= (p.Glu489=)
c.1558G= (p.Glu520=)
c.169+8357C= (p.=)
c.*124+8156C= (p.=)
c.*1202G= (p.=)
c.949G= (p.Glu317=)
c.1852G= (p.Glu618=)
c.-1242G= (p.=)
c.1672G= (p.Glu558=)
2g.47799838G>TCA346749765MSH6c.1855G>T (p.Glu619Ter)
c.1465G>T (p.Glu489Ter)
c.1558G>T (p.Glu520Ter)
c.169+8357C>A (p.=)
c.*124+8156C>A (p.=)
c.*1202G>T (p.=)
c.949G>T (p.Glu317Ter)
c.1852G>T (p.Glu618Ter)
c.-1242G>T (p.=)
c.1672G>T (p.Glu558Ter)
ClinVar COSMIC
2g.47799839A>CCA346749769MSH6c.1856A>C (p.Glu619Ala)
c.1466A>C (p.Glu489Ala)
c.1559A>C (p.Glu520Ala)
c.169+8356T>G (p.=)
c.*124+8155T>G (p.=)
c.*1203A>C (p.=)
c.950A>C (p.Glu317Ala)
c.1853A>C (p.Glu618Ala)
c.-1241A>C (p.=)
c.1673A>C (p.Glu558Ala)
2g.47799839A>GCA346749772MSH6c.1856A>G (p.Glu619Gly)
c.1466A>G (p.Glu489Gly)
c.1559A>G (p.Glu520Gly)
c.169+8356T>C (p.=)
c.*124+8155T>C (p.=)
c.*1203A>G (p.=)
c.950A>G (p.Glu317Gly)
c.1853A>G (p.Glu618Gly)
c.-1241A>G (p.=)
c.1673A>G (p.Glu558Gly)
2g.47799839A>TCA346749778MSH6c.1856A>T (p.Glu619Val)
c.1466A>T (p.Glu489Val)
c.1559A>T (p.Glu520Val)
c.169+8356T>A (p.=)
c.*124+8155T>A (p.=)
c.*1203A>T (p.=)
c.950A>T (p.Glu317Val)
c.1853A>T (p.Glu618Val)
c.-1241A>T (p.=)
c.1673A>T (p.Glu558Val)
2g.47799840A=CA2496049046MSH6c.1857A= (p.Glu619=)
c.1467A= (p.Glu489=)
c.1560A= (p.Glu520=)
c.169+8355T= (p.=)
c.*124+8154T= (p.=)
c.*1204A= (p.=)
c.951A= (p.Glu317=)
c.1854A= (p.Glu618=)
c.-1240A= (p.=)
c.1674A= (p.Glu558=)
2g.47799840A>CCA009330MSH6c.1857A>C (p.Glu619Asp)
c.1467A>C (p.Glu489Asp)
c.1560A>C (p.Glu520Asp)
c.169+8355T>G (p.=)
c.*124+8154T>G (p.=)
c.*1204A>C (p.=)
c.951A>C (p.Glu317Asp)
c.1854A>C (p.Glu618Asp)
c.-1240A>C (p.=)
c.1674A>C (p.Glu558Asp)
ClinVar dbSNP ExAC gnomAD
2g.47799840A>GCA426121258MSH6c.1857A>G (p.Glu619=)
c.1467A>G (p.Glu489=)
c.1560A>G (p.Glu520=)
c.169+8355T>C (p.=)
c.*124+8154T>C (p.=)
c.*1204A>G (p.=)
c.951A>G (p.Glu317=)
c.1854A>G (p.Glu618=)
c.-1240A>G (p.=)
c.1674A>G (p.Glu558=)
2g.47799840A>TCA346749794MSH6c.1857A>T (p.Glu619Asp)
c.1467A>T (p.Glu489Asp)
c.1560A>T (p.Glu520Asp)
c.169+8355T>A (p.=)
c.*124+8154T>A (p.=)
c.*1204A>T (p.=)
c.951A>T (p.Glu317Asp)
c.1854A>T (p.Glu618Asp)
c.-1240A>T (p.=)
c.1674A>T (p.Glu558Asp)
2g.47799841G>ACA10577265MSH6c.1858G>A (p.Gly620Ser)
c.1468G>A (p.Gly490Ser)
c.1561G>A (p.Gly521Ser)
c.169+8354C>T (p.=)
c.*124+8153C>T (p.=)
c.*1205G>A (p.=)
c.952G>A (p.Gly318Ser)
c.1855G>A (p.Gly619Ser)
c.-1239G>A (p.=)
c.1675G>A (p.Gly559Ser)
ClinVar dbSNP gnomAD COSMIC
2g.47799841G>CCA346749799MSH6c.1858G>C (p.Gly620Arg)
c.1468G>C (p.Gly490Arg)
c.1561G>C (p.Gly521Arg)
c.169+8354C>G (p.=)
c.*124+8153C>G (p.=)
c.*1205G>C (p.=)
c.952G>C (p.Gly318Arg)
c.1855G>C (p.Gly619Arg)
c.-1239G>C (p.=)
c.1675G>C (p.Gly559Arg)
2g.47799841G=CA2496049047MSH6c.1858G= (p.Gly620=)
c.1468G= (p.Gly490=)
c.1561G= (p.Gly521=)
c.169+8354C= (p.=)
c.*124+8153C= (p.=)
c.*1205G= (p.=)
c.952G= (p.Gly318=)
c.1855G= (p.Gly619=)
c.-1239G= (p.=)
c.1675G= (p.Gly559=)
2g.47799841G>TCA346749808MSH6c.1858G>T (p.Gly620Cys)
c.1468G>T (p.Gly490Cys)
c.1561G>T (p.Gly521Cys)
c.169+8354C>A (p.=)
c.*124+8153C>A (p.=)
c.*1205G>T (p.=)
c.952G>T (p.Gly318Cys)
c.1855G>T (p.Gly619Cys)
c.-1239G>T (p.=)
c.1675G>T (p.Gly559Cys)
ClinVar
2g.47799842G>ACA346749813MSH6c.1859G>A (p.Gly620Asp)
c.1469G>A (p.Gly490Asp)
c.1562G>A (p.Gly521Asp)
c.169+8353C>T (p.=)
c.*124+8152C>T (p.=)
c.*1206G>A (p.=)
c.953G>A (p.Gly318Asp)
c.1856G>A (p.Gly619Asp)
c.-1238G>A (p.=)
c.1676G>A (p.Gly559Asp)
2g.47799842G>CCA346749816MSH6c.1859G>C (p.Gly620Ala)
c.1469G>C (p.Gly490Ala)
c.1562G>C (p.Gly521Ala)
c.169+8353C>G (p.=)
c.*124+8152C>G (p.=)
c.*1206G>C (p.=)
c.953G>C (p.Gly318Ala)
c.1856G>C (p.Gly619Ala)
c.-1238G>C (p.=)
c.1676G>C (p.Gly559Ala)
ClinVar
2g.47799842G=CA2496049048MSH6c.1859G= (p.Gly620=)
c.1469G= (p.Gly490=)
c.1562G= (p.Gly521=)
c.169+8353C= (p.=)
c.*124+8152C= (p.=)
c.*1206G= (p.=)
c.953G= (p.Gly318=)
c.1856G= (p.Gly619=)
c.-1238G= (p.=)
c.1676G= (p.Gly559=)
2g.47799842G>TCA346749823MSH6c.1859G>T (p.Gly620Val)
c.1469G>T (p.Gly490Val)
c.1562G>T (p.Gly521Val)
c.169+8353C>A (p.=)
c.*124+8152C>A (p.=)
c.*1206G>T (p.=)
c.953G>T (p.Gly318Val)
c.1856G>T (p.Gly619Val)
c.-1238G>T (p.=)
c.1676G>T (p.Gly559Val)

Number of alleles fetched