Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.61928260G>ACA511322150CDH4c.1842G>A (p.Glu614=)
c.1620G>A (p.Glu540=)
c.1560G>A (p.Glu520=)
c.1731G>A (p.Glu577=)
20g.61928260G>CCA409508849CDH4c.1842G>C (p.Glu614Asp)
c.1620G>C (p.Glu540Asp)
c.1560G>C (p.Glu520Asp)
c.1731G>C (p.Glu577Asp)
20g.61928260G>TCA409508850CDH4c.1842G>T (p.Glu614Asp)
c.1620G>T (p.Glu540Asp)
c.1560G>T (p.Glu520Asp)
c.1731G>T (p.Glu577Asp)
 gnomAD v4
20g.61928261C>ACA409508851CDH4c.1843C>A (p.Leu615Met)
c.1621C>A (p.Leu541Met)
c.1561C>A (p.Leu521Met)
c.1732C>A (p.Leu578Met)
 gnomAD v4
20g.61928261C=CA2373989225CDH4c.1843C= (p.Leu615=)
c.1621C= (p.Leu541=)
c.1561C= (p.Leu521=)
c.1732C= (p.Leu578=)
20g.61928261C>GCA409508853CDH4c.1843C>G (p.Leu615Val)
c.1621C>G (p.Leu541Val)
c.1561C>G (p.Leu521Val)
c.1732C>G (p.Leu578Val)
20g.61928261C>TCA511322151CDH4c.1843C>T (p.Leu615=)
c.1621C>T (p.Leu541=)
c.1561C>T (p.Leu521=)
c.1732C>T (p.Leu578=)
 dbSNP gnomAD v2 gnomAD v4
20g.61928262T>ACA409508858CDH4c.1844T>A (p.Leu615Gln)
c.1622T>A (p.Leu541Gln)
c.1562T>A (p.Leu521Gln)
c.1733T>A (p.Leu578Gln)
20g.61928262T>CCA9934885CDH4c.1844T>C (p.Leu615Pro)
c.1622T>C (p.Leu541Pro)
c.1562T>C (p.Leu521Pro)
c.1733T>C (p.Leu578Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928262T>GCA409508855CDH4c.1844T>G (p.Leu615Arg)
c.1622T>G (p.Leu541Arg)
c.1562T>G (p.Leu521Arg)
c.1733T>G (p.Leu578Arg)
20g.61928262T=CA2373989226CDH4c.1844T= (p.Leu615=)
c.1622T= (p.Leu541=)
c.1562T= (p.Leu521=)
c.1733T= (p.Leu578=)
20g.61928263G>ACA511322152CDH4c.1845G>A (p.Leu615=)
c.1623G>A (p.Leu541=)
c.1563G>A (p.Leu521=)
c.1734G>A (p.Leu578=)
 dbSNP gnomAD v2
20g.61928263G>CCA511322153CDH4c.1845G>C (p.Leu615=)
c.1623G>C (p.Leu541=)
c.1563G>C (p.Leu521=)
c.1734G>C (p.Leu578=)
20g.61928263G=CA2373989227CDH4c.1845G= (p.Leu615=)
c.1623G= (p.Leu541=)
c.1563G= (p.Leu521=)
c.1734G= (p.Leu578=)
20g.61928263G>TCA511322154CDH4c.1845G>T (p.Leu615=)
c.1623G>T (p.Leu541=)
c.1563G>T (p.Leu521=)
c.1734G>T (p.Leu578=)
 gnomAD v4
20g.61928264C>ACA409508862CDH4c.1846C>A (p.Leu616Met)
c.1624C>A (p.Leu542Met)
c.1564C>A (p.Leu522Met)
c.1735C>A (p.Leu579Met)
20g.61928264C>GCA409508860CDH4c.1846C>G (p.Leu616Val)
c.1624C>G (p.Leu542Val)
c.1564C>G (p.Leu522Val)
c.1735C>G (p.Leu579Val)
20g.61928264C>TCA511322155CDH4c.1846C>T (p.Leu616=)
c.1624C>T (p.Leu542=)
c.1564C>T (p.Leu522=)
c.1735C>T (p.Leu579=)
 gnomAD v4
20g.61928265T>ACA409508866CDH4c.1847T>A (p.Leu616Gln)
c.1625T>A (p.Leu542Gln)
c.1565T>A (p.Leu522Gln)
c.1736T>A (p.Leu579Gln)
20g.61928265T>CCA409508865CDH4c.1847T>C (p.Leu616Pro)
c.1625T>C (p.Leu542Pro)
c.1565T>C (p.Leu522Pro)
c.1736T>C (p.Leu579Pro)
20g.61928265T>GCA409508868CDH4c.1847T>G (p.Leu616Arg)
c.1625T>G (p.Leu542Arg)
c.1565T>G (p.Leu522Arg)
c.1736T>G (p.Leu579Arg)
20g.61928266G>ACA511322156CDH4c.1848G>A (p.Leu616=)
c.1626G>A (p.Leu542=)
c.1566G>A (p.Leu522=)
c.1737G>A (p.Leu579=)
 dbSNP gnomAD v4
20g.61928266G>CCA511322157CDH4c.1848G>C (p.Leu616=)
c.1626G>C (p.Leu542=)
c.1566G>C (p.Leu522=)
c.1737G>C (p.Leu579=)
20g.61928266G>TCA511322158CDH4c.1848G>T (p.Leu616=)
c.1626G>T (p.Leu542=)
c.1566G>T (p.Leu522=)
c.1737G>T (p.Leu579=)
 gnomAD v4
20g.61928267C>ACA409508871CDH4c.1849C>A (p.Pro617Thr)
c.1627C>A (p.Pro543Thr)
c.1567C>A (p.Pro523Thr)
c.1738C>A (p.Pro580Thr)
 gnomAD v4
20g.61928267C>GCA409508872CDH4c.1849C>G (p.Pro617Ala)
c.1627C>G (p.Pro543Ala)
c.1567C>G (p.Pro523Ala)
c.1738C>G (p.Pro580Ala)
20g.61928267C>TCA409508874CDH4c.1849C>T (p.Pro617Ser)
c.1627C>T (p.Pro543Ser)
c.1567C>T (p.Pro523Ser)
c.1738C>T (p.Pro580Ser)
 gnomAD v4 COSMIC
20g.61928268C>ACA409508876CDH4c.1850C>A (p.Pro617His)
c.1628C>A (p.Pro543His)
c.1568C>A (p.Pro523His)
c.1739C>A (p.Pro580His)
20g.61928268C=CA2373989228CDH4c.1850C= (p.Pro617=)
c.1628C= (p.Pro543=)
c.1568C= (p.Pro523=)
c.1739C= (p.Pro580=)
20g.61928268C>GCA409508878CDH4c.1850C>G (p.Pro617Arg)
c.1628C>G (p.Pro543Arg)
c.1568C>G (p.Pro523Arg)
c.1739C>G (p.Pro580Arg)
 gnomAD v4
20g.61928268C>TCA409508879CDH4c.1850C>T (p.Pro617Leu)
c.1628C>T (p.Pro543Leu)
c.1568C>T (p.Pro523Leu)
c.1739C>T (p.Pro580Leu)
 dbSNP
20g.61928269C>ACA511322161CDH4c.1851C>A (p.Pro617=)
c.1629C>A (p.Pro543=)
c.1569C>A (p.Pro523=)
c.1740C>A (p.Pro580=)
 gnomAD v4
20g.61928269C=CA2373989229CDH4c.1851C= (p.Pro617=)
c.1629C= (p.Pro543=)
c.1569C= (p.Pro523=)
c.1740C= (p.Pro580=)
20g.61928269C>GCA511322163CDH4c.1851C>G (p.Pro617=)
c.1629C>G (p.Pro543=)
c.1569C>G (p.Pro523=)
c.1740C>G (p.Pro580=)
20g.61928269C>TCA511322164CDH4c.1851C>T (p.Pro617=)
c.1629C>T (p.Pro543=)
c.1569C>T (p.Pro523=)
c.1740C>T (p.Pro580=)
 dbSNP gnomAD v4
20g.61928270A=CA2373989230CDH4c.1852A= (p.Lys618=)
c.1630A= (p.Lys544=)
c.1570A= (p.Lys524=)
c.1741A= (p.Lys581=)
20g.61928270A>CCA409508882CDH4c.1852A>C (p.Lys618Gln)
c.1630A>C (p.Lys544Gln)
c.1570A>C (p.Lys524Gln)
c.1741A>C (p.Lys581Gln)
20g.61928270A>GCA409508883CDH4c.1852A>G (p.Lys618Glu)
c.1630A>G (p.Lys544Glu)
c.1570A>G (p.Lys524Glu)
c.1741A>G (p.Lys581Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928270A>TCA409508885CDH4c.1852A>T (p.Lys618Ter)
c.1630A>T (p.Lys544Ter)
c.1570A>T (p.Lys524Ter)
c.1741A>T (p.Lys581Ter)
20g.61928271delCA2653589342CDH4c.1853del (p.Lys618ArgfsTer11)
c.1631del (p.Lys544ArgfsTer11)
c.1571del (p.Lys524ArgfsTer11)
c.1742del (p.Lys581ArgfsTer11)
 gnomAD v4
20g.61928271A=CA2373989231CDH4c.1853A= (p.Lys618=)
c.1631A= (p.Lys544=)
c.1571A= (p.Lys524=)
c.1742A= (p.Lys581=)
20g.61928271A>CCA409508888CDH4c.1853A>C (p.Lys618Thr)
c.1631A>C (p.Lys544Thr)
c.1571A>C (p.Lys524Thr)
c.1742A>C (p.Lys581Thr)
 COSMIC
20g.61928271A>GCA409508890CDH4c.1853A>G (p.Lys618Arg)
c.1631A>G (p.Lys544Arg)
c.1571A>G (p.Lys524Arg)
c.1742A>G (p.Lys581Arg)
 dbSNP gnomAD v2 gnomAD v4
20g.61928271A>TCA409508891CDH4c.1853A>T (p.Lys618Met)
c.1631A>T (p.Lys544Met)
c.1571A>T (p.Lys524Met)
c.1742A>T (p.Lys581Met)
20g.61928272G>ACA511322168CDH4c.1854G>A (p.Lys618=)
c.1632G>A (p.Lys544=)
c.1572G>A (p.Lys524=)
c.1743G>A (p.Lys581=)
 dbSNP gnomAD v3 gnomAD v4
20g.61928272G>CCA409508893CDH4c.1854G>C (p.Lys618Asn)
c.1632G>C (p.Lys544Asn)
c.1572G>C (p.Lys524Asn)
c.1743G>C (p.Lys581Asn)
 ClinVar dbSNP gnomAD v3 gnomAD v4
20g.61928272G=CA2373989232CDH4c.1854G= (p.Lys618=)
c.1632G= (p.Lys544=)
c.1572G= (p.Lys524=)
c.1743G= (p.Lys581=)
20g.61928272G>TCA409508895CDH4c.1854G>T (p.Lys618Asn)
c.1632G>T (p.Lys544Asn)
c.1572G>T (p.Lys524Asn)
c.1743G>T (p.Lys581Asn)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928273G>ACA409508897CDH4c.1855G>A (p.Glu619Lys)
c.1633G>A (p.Glu545Lys)
c.1573G>A (p.Glu525Lys)
c.1744G>A (p.Glu582Lys)
 COSMIC
20g.61928273G>CCA409508899CDH4c.1855G>C (p.Glu619Gln)
c.1633G>C (p.Glu545Gln)
c.1573G>C (p.Glu525Gln)
c.1744G>C (p.Glu582Gln)
20g.61928273G>TCA409508901CDH4c.1855G>T (p.Glu619Ter)
c.1633G>T (p.Glu545Ter)
c.1573G>T (p.Glu525Ter)
c.1744G>T (p.Glu582Ter)
 gnomAD v4
20g.61928274A>CCA409508903CDH4c.1856A>C (p.Glu619Ala)
c.1634A>C (p.Glu545Ala)
c.1574A>C (p.Glu525Ala)
c.1745A>C (p.Glu582Ala)
20g.61928274A>GCA409508905CDH4c.1856A>G (p.Glu619Gly)
c.1634A>G (p.Glu545Gly)
c.1574A>G (p.Glu525Gly)
c.1745A>G (p.Glu582Gly)
20g.61928274A>TCA409508907CDH4c.1856A>T (p.Glu619Val)
c.1634A>T (p.Glu545Val)
c.1574A>T (p.Glu525Val)
c.1745A>T (p.Glu582Val)
20g.61928275G>ACA511322169CDH4c.1857G>A (p.Glu619=)
c.1635G>A (p.Glu545=)
c.1575G>A (p.Glu525=)
c.1746G>A (p.Glu582=)
 dbSNP gnomAD v4
20g.61928275G>CCA409508909CDH4c.1857G>C (p.Glu619Asp)
c.1635G>C (p.Glu545Asp)
c.1575G>C (p.Glu525Asp)
c.1746G>C (p.Glu582Asp)
20g.61928275G>TCA409508911CDH4c.1857G>T (p.Glu619Asp)
c.1635G>T (p.Glu545Asp)
c.1575G>T (p.Glu525Asp)
c.1746G>T (p.Glu582Asp)
20g.61928276G>ACA409508913CDH4c.1858G>A (p.Ala620Thr)
c.1636G>A (p.Ala546Thr)
c.1576G>A (p.Ala526Thr)
c.1747G>A (p.Ala583Thr)
20g.61928276G>CCA409508915CDH4c.1858G>C (p.Ala620Pro)
c.1636G>C (p.Ala546Pro)
c.1576G>C (p.Ala526Pro)
c.1747G>C (p.Ala583Pro)
20g.61928276G>TCA409508917CDH4c.1858G>T (p.Ala620Ser)
c.1636G>T (p.Ala546Ser)
c.1576G>T (p.Ala526Ser)
c.1747G>T (p.Ala583Ser)
 gnomAD v4
20g.61928277C>ACA409508920CDH4c.1859C>A (p.Ala620Glu)
c.1637C>A (p.Ala546Glu)
c.1577C>A (p.Ala526Glu)
c.1748C>A (p.Ala583Glu)
 gnomAD v4
20g.61928277C=CA2373989233CDH4c.1859C= (p.Ala620=)
c.1637C= (p.Ala546=)
c.1577C= (p.Ala526=)
c.1748C= (p.Ala583=)
20g.61928277C>GCA409508922CDH4c.1859C>G (p.Ala620Gly)
c.1637C>G (p.Ala546Gly)
c.1577C>G (p.Ala526Gly)
c.1748C>G (p.Ala583Gly)
 gnomAD v4
20g.61928277C>TCA9934886CDH4c.1859C>T (p.Ala620Val)
c.1637C>T (p.Ala546Val)
c.1577C>T (p.Ala526Val)
c.1748C>T (p.Ala583Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928278G>ACA9934887CDH4c.1860G>A (p.Ala620=)
c.1638G>A (p.Ala546=)
c.1578G>A (p.Ala526=)
c.1749G>A (p.Ala583=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928278G>CCA511322172CDH4c.1860G>C (p.Ala620=)
c.1638G>C (p.Ala546=)
c.1578G>C (p.Ala526=)
c.1749G>C (p.Ala583=)
20g.61928278G=CA2373989234CDH4c.1860G= (p.Ala620=)
c.1638G= (p.Ala546=)
c.1578G= (p.Ala526=)
c.1749G= (p.Ala583=)
20g.61928278G>TCA511322173CDH4c.1860G>T (p.Ala620=)
c.1638G>T (p.Ala546=)
c.1578G>T (p.Ala526=)
c.1749G>T (p.Ala583=)
 gnomAD v4
20g.61928279C>ACA409508925CDH4c.1861C>A (p.Gln621Lys)
c.1639C>A (p.Gln547Lys)
c.1579C>A (p.Gln527Lys)
c.1750C>A (p.Gln584Lys)
 dbSNP gnomAD v4
20g.61928279C>GCA409508927CDH4c.1861C>G (p.Gln621Glu)
c.1639C>G (p.Gln547Glu)
c.1579C>G (p.Gln527Glu)
c.1750C>G (p.Gln584Glu)
20g.61928279C>TCA409508929CDH4c.1861C>T (p.Gln621Ter)
c.1639C>T (p.Gln547Ter)
c.1579C>T (p.Gln527Ter)
c.1750C>T (p.Gln584Ter)
20g.61928280A>CCA409508931CDH4c.1862A>C (p.Gln621Pro)
c.1640A>C (p.Gln547Pro)
c.1580A>C (p.Gln527Pro)
c.1751A>C (p.Gln584Pro)
20g.61928280A>GCA409508933CDH4c.1862A>G (p.Gln621Arg)
c.1640A>G (p.Gln547Arg)
c.1580A>G (p.Gln527Arg)
c.1751A>G (p.Gln584Arg)
20g.61928280A>TCA409508935CDH4c.1862A>T (p.Gln621Leu)
c.1640A>T (p.Gln547Leu)
c.1580A>T (p.Gln527Leu)
c.1751A>T (p.Gln584Leu)
20g.61928281G>ACA511322177CDH4c.1863G>A (p.Gln621=)
c.1641G>A (p.Gln547=)
c.1581G>A (p.Gln527=)
c.1752G>A (p.Gln584=)
20g.61928281G>CCA409508937CDH4c.1863G>C (p.Gln621His)
c.1641G>C (p.Gln547His)
c.1581G>C (p.Gln527His)
c.1752G>C (p.Gln584His)
20g.61928281G=CA2373989235CDH4c.1863G= (p.Gln621=)
c.1641G= (p.Gln547=)
c.1581G= (p.Gln527=)
c.1752G= (p.Gln584=)
20g.61928281G>TCA9934888CDH4c.1863G>T (p.Gln621His)
c.1641G>T (p.Gln547His)
c.1581G>T (p.Gln527His)
c.1752G>T (p.Gln584His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928282A=CA2373989236CDH4c.1864A= (p.Ile622=)
c.1642A= (p.Ile548=)
c.1582A= (p.Ile528=)
c.1753A= (p.Ile585=)
20g.61928282A>CCA409508941CDH4c.1864A>C (p.Ile622Leu)
c.1642A>C (p.Ile548Leu)
c.1582A>C (p.Ile528Leu)
c.1753A>C (p.Ile585Leu)
20g.61928282A>GCA409508943CDH4c.1864A>G (p.Ile622Val)
c.1642A>G (p.Ile548Val)
c.1582A>G (p.Ile528Val)
c.1753A>G (p.Ile585Val)
 dbSNP gnomAD v2 gnomAD v4
20g.61928282A>TCA9934889CDH4c.1864A>T (p.Ile622Phe)
c.1642A>T (p.Ile548Phe)
c.1582A>T (p.Ile528Phe)
c.1753A>T (p.Ile585Phe)
 dbSNP ExAC gnomAD v3 gnomAD v4
20g.61928283T>ACA409508951CDH4c.1865T>A (p.Ile622Asn)
c.1643T>A (p.Ile548Asn)
c.1583T>A (p.Ile528Asn)
c.1754T>A (p.Ile585Asn)
20g.61928283T>CCA409508946CDH4c.1865T>C (p.Ile622Thr)
c.1643T>C (p.Ile548Thr)
c.1583T>C (p.Ile528Thr)
c.1754T>C (p.Ile585Thr)
 dbSNP gnomAD v4
20g.61928283T>GCA409508949CDH4c.1865T>G (p.Ile622Ser)
c.1643T>G (p.Ile548Ser)
c.1583T>G (p.Ile528Ser)
c.1754T>G (p.Ile585Ser)
20g.61928283T=CA2373989237CDH4c.1865T= (p.Ile622=)
c.1643T= (p.Ile548=)
c.1583T= (p.Ile528=)
c.1754T= (p.Ile585=)
20g.61928284C>ACA511322181CDH4c.1866C>A (p.Ile622=)
c.1644C>A (p.Ile548=)
c.1584C>A (p.Ile528=)
c.1755C>A (p.Ile585=)
20g.61928284C>GCA409508953CDH4c.1866C>G (p.Ile622Met)
c.1644C>G (p.Ile548Met)
c.1584C>G (p.Ile528Met)
c.1755C>G (p.Ile585Met)
20g.61928284C>TCA511322182CDH4c.1866C>T (p.Ile622=)
c.1644C>T (p.Ile548=)
c.1584C>T (p.Ile528=)
c.1755C>T (p.Ile585=)
 gnomAD v4
20g.61928285T>ACA409508955CDH4c.1867T>A (p.Cys623Ser)
c.1645T>A (p.Cys549Ser)
c.1585T>A (p.Cys529Ser)
c.1756T>A (p.Cys586Ser)
20g.61928285T>CCA9934890CDH4c.1867T>C (p.Cys623Arg)
c.1645T>C (p.Cys549Arg)
c.1585T>C (p.Cys529Arg)
c.1756T>C (p.Cys586Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928285T>GCA409508958CDH4c.1867T>G (p.Cys623Gly)
c.1645T>G (p.Cys549Gly)
c.1585T>G (p.Cys529Gly)
c.1756T>G (p.Cys586Gly)
20g.61928285T=CA2373989238CDH4c.1867T= (p.Cys623=)
c.1645T= (p.Cys549=)
c.1585T= (p.Cys529=)
c.1756T= (p.Cys586=)
20g.61928286G>ACA409508960CDH4c.1868G>A (p.Cys623Tyr)
c.1646G>A (p.Cys549Tyr)
c.1586G>A (p.Cys529Tyr)
c.1757G>A (p.Cys586Tyr)
20g.61928286G>CCA409508961CDH4c.1868G>C (p.Cys623Ser)
c.1646G>C (p.Cys549Ser)
c.1586G>C (p.Cys529Ser)
c.1757G>C (p.Cys586Ser)
20g.61928286G>TCA409508963CDH4c.1868G>T (p.Cys623Phe)
c.1646G>T (p.Cys549Phe)
c.1586G>T (p.Cys529Phe)
c.1757G>T (p.Cys586Phe)
 gnomAD v4
20g.61928287C>ACA409508966CDH4c.1869C>A (p.Cys623Ter)
c.1647C>A (p.Cys549Ter)
c.1587C>A (p.Cys529Ter)
c.1758C>A (p.Cys586Ter)
 COSMIC
20g.61928287C=CA2373989239CDH4c.1869C= (p.Cys623=)
c.1647C= (p.Cys549=)
c.1587C= (p.Cys529=)
c.1758C= (p.Cys586=)
20g.61928287C>GCA409508967CDH4c.1869C>G (p.Cys623Trp)
c.1647C>G (p.Cys549Trp)
c.1587C>G (p.Cys529Trp)
c.1758C>G (p.Cys586Trp)
20g.61928287C>TCA9934891CDH4c.1869C>T (p.Cys623=)
c.1647C>T (p.Cys549=)
c.1587C>T (p.Cys529=)
c.1758C>T (p.Cys586=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928288G>ACA9934892CDH4c.1870G>A (p.Glu624Lys)
c.1648G>A (p.Glu550Lys)
c.1588G>A (p.Glu530Lys)
c.1759G>A (p.Glu587Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928288G>CCA409508970CDH4c.1870G>C (p.Glu624Gln)
c.1648G>C (p.Glu550Gln)
c.1588G>C (p.Glu530Gln)
c.1759G>C (p.Glu587Gln)
 gnomAD v3 gnomAD v4
20g.61928288G=CA2373989240CDH4c.1870G= (p.Glu624=)
c.1648G= (p.Glu550=)
c.1588G= (p.Glu530=)
c.1759G= (p.Glu587=)
20g.61928288G>TCA409508972CDH4c.1870G>T (p.Glu624Ter)
c.1648G>T (p.Glu550Ter)
c.1588G>T (p.Glu530Ter)
c.1759G>T (p.Glu587Ter)
 gnomAD v4
20g.61928288_61928291delinsGAGACA2373989241CDH4c.1870_1873delinsGAGA (p.Glu624=)
c.1648_1651delinsGAGA (p.Glu550=)
c.1588_1591delinsGAGA (p.Glu530=)
c.1759_1762delinsGAGA (p.Glu587=)
20g.61928289A>CCA409508978CDH4c.1871A>C (p.Glu624Ala)
c.1649A>C (p.Glu550Ala)
c.1589A>C (p.Glu530Ala)
c.1760A>C (p.Glu587Ala)
20g.61928289A>GCA409508980CDH4c.1871A>G (p.Glu624Gly)
c.1649A>G (p.Glu550Gly)
c.1589A>G (p.Glu530Gly)
c.1760A>G (p.Glu587Gly)
20g.61928289A>TCA409508976CDH4c.1871A>T (p.Glu624Val)
c.1649A>T (p.Glu550Val)
c.1589A>T (p.Glu530Val)
c.1760A>T (p.Glu587Val)
20g.61928291_61928293delCA2373989242CDH4c.1873_1875del (p.Lys625del)
c.1651_1653del (p.Lys551del)
c.1591_1593del (p.Lys531del)
c.1762_1764del (p.Lys588del)
 dbSNP gnomAD v4
20g.61928290G>ACA511322186CDH4c.1872G>A (p.Glu624=)
c.1650G>A (p.Glu550=)
c.1590G>A (p.Glu530=)
c.1761G>A (p.Glu587=)
 gnomAD v4
20g.61928290G>CCA409508984CDH4c.1872G>C (p.Glu624Asp)
c.1650G>C (p.Glu550Asp)
c.1590G>C (p.Glu530Asp)
c.1761G>C (p.Glu587Asp)
20g.61928290G>TCA409508982CDH4c.1872G>T (p.Glu624Asp)
c.1650G>T (p.Glu550Asp)
c.1590G>T (p.Glu530Asp)
c.1761G>T (p.Glu587Asp)
 gnomAD v4
20g.61928291A=CA2373989243CDH4c.1873A= (p.Lys625=)
c.1651A= (p.Lys551=)
c.1591A= (p.Lys531=)
c.1762A= (p.Lys588=)
20g.61928291A>CCA409508985CDH4c.1873A>C (p.Lys625Gln)
c.1651A>C (p.Lys551Gln)
c.1591A>C (p.Lys531Gln)
c.1762A>C (p.Lys588Gln)
20g.61928291A>GCA409508987CDH4c.1873A>G (p.Lys625Glu)
c.1651A>G (p.Lys551Glu)
c.1591A>G (p.Lys531Glu)
c.1762A>G (p.Lys588Glu)
 dbSNP gnomAD v4
20g.61928291A>TCA409508989CDH4c.1873A>T (p.Lys625Ter)
c.1651A>T (p.Lys551Ter)
c.1591A>T (p.Lys531Ter)
c.1762A>T (p.Lys588Ter)
20g.61928292A=CA2373989244CDH4c.1874A= (p.Lys625=)
c.1652A= (p.Lys551=)
c.1592A= (p.Lys531=)
c.1763A= (p.Lys588=)
20g.61928292A>CCA409508991CDH4c.1874A>C (p.Lys625Thr)
c.1652A>C (p.Lys551Thr)
c.1592A>C (p.Lys531Thr)
c.1763A>C (p.Lys588Thr)
20g.61928292A>GCA9934893CDH4c.1874A>G (p.Lys625Arg)
c.1652A>G (p.Lys551Arg)
c.1592A>G (p.Lys531Arg)
c.1763A>G (p.Lys588Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928292A>TCA409508994CDH4c.1874A>T (p.Lys625Met)
c.1652A>T (p.Lys551Met)
c.1592A>T (p.Lys531Met)
c.1763A>T (p.Lys588Met)
 dbSNP gnomAD v4
20g.61928293G>ACA511322190CDH4c.1875G>A (p.Lys625=)
c.1653G>A (p.Lys551=)
c.1593G>A (p.Lys531=)
c.1764G>A (p.Lys588=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928293G>CCA409508996CDH4c.1875G>C (p.Lys625Asn)
c.1653G>C (p.Lys551Asn)
c.1593G>C (p.Lys531Asn)
c.1764G>C (p.Lys588Asn)
20g.61928293G=CA2373989245CDH4c.1875G= (p.Lys625=)
c.1653G= (p.Lys551=)
c.1593G= (p.Lys531=)
c.1764G= (p.Lys588=)
20g.61928293G>TCA409508998CDH4c.1875G>T (p.Lys625Asn)
c.1653G>T (p.Lys551Asn)
c.1593G>T (p.Lys531Asn)
c.1764G>T (p.Lys588Asn)
 gnomAD v4
20g.61928294C>ACA409509001CDH4c.1876C>A (p.Pro626Thr)
c.1654C>A (p.Pro552Thr)
c.1594C>A (p.Pro532Thr)
c.1765C>A (p.Pro589Thr)
 ClinVar gnomAD v4
20g.61928294C=CA2373989246CDH4c.1876C= (p.Pro626=)
c.1654C= (p.Pro552=)
c.1594C= (p.Pro532=)
c.1765C= (p.Pro589=)
20g.61928294C>GCA409509002CDH4c.1876C>G (p.Pro626Ala)
c.1654C>G (p.Pro552Ala)
c.1594C>G (p.Pro532Ala)
c.1765C>G (p.Pro589Ala)
20g.61928294C>TCA409509004CDH4c.1876C>T (p.Pro626Ser)
c.1654C>T (p.Pro552Ser)
c.1594C>T (p.Pro532Ser)
c.1765C>T (p.Pro589Ser)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
20g.61928295C>ACA409509008CDH4c.1877C>A (p.Pro626His)
c.1655C>A (p.Pro552His)
c.1595C>A (p.Pro532His)
c.1766C>A (p.Pro589His)
 gnomAD v4
20g.61928295C=CA2373989247CDH4c.1877C= (p.Pro626=)
c.1655C= (p.Pro552=)
c.1595C= (p.Pro532=)
c.1766C= (p.Pro589=)
20g.61928295C>GCA409509010CDH4c.1877C>G (p.Pro626Arg)
c.1655C>G (p.Pro552Arg)
c.1595C>G (p.Pro532Arg)
c.1766C>G (p.Pro589Arg)
20g.61928295C>TCA409509007CDH4c.1877C>T (p.Pro626Leu)
c.1655C>T (p.Pro552Leu)
c.1595C>T (p.Pro532Leu)
c.1766C>T (p.Pro589Leu)
 dbSNP gnomAD v2
20g.61928296C>ACA511322192CDH4c.1878C>A (p.Pro626=)
c.1656C>A (p.Pro552=)
c.1596C>A (p.Pro532=)
c.1767C>A (p.Pro589=)
 gnomAD v4
20g.61928296C>GCA511322193CDH4c.1878C>G (p.Pro626=)
c.1656C>G (p.Pro552=)
c.1596C>G (p.Pro532=)
c.1767C>G (p.Pro589=)
20g.61928296C>TCA511322195CDH4c.1878C>T (p.Pro626=)
c.1656C>T (p.Pro552=)
c.1596C>T (p.Pro532=)
c.1767C>T (p.Pro589=)
20g.61928297A>CCA409509012CDH4c.1879A>C (p.Asn627His)
c.1657A>C (p.Asn553His)
c.1597A>C (p.Asn533His)
c.1768A>C (p.Asn590His)
20g.61928297A>GCA409509014CDH4c.1879A>G (p.Asn627Asp)
c.1657A>G (p.Asn553Asp)
c.1597A>G (p.Asn533Asp)
c.1768A>G (p.Asn590Asp)
 gnomAD v4
20g.61928297A>TCA409509016CDH4c.1879A>T (p.Asn627Tyr)
c.1657A>T (p.Asn553Tyr)
c.1597A>T (p.Asn533Tyr)
c.1768A>T (p.Asn590Tyr)
20g.61928298A=CA2373989248CDH4c.1880A= (p.Asn627=)
c.1658A= (p.Asn553=)
c.1598A= (p.Asn533=)
c.1769A= (p.Asn590=)
20g.61928298A>CCA409509018CDH4c.1880A>C (p.Asn627Thr)
c.1658A>C (p.Asn553Thr)
c.1598A>C (p.Asn533Thr)
c.1769A>C (p.Asn590Thr)
20g.61928298A>GCA409509020CDH4c.1880A>G (p.Asn627Ser)
c.1658A>G (p.Asn553Ser)
c.1598A>G (p.Asn533Ser)
c.1769A>G (p.Asn590Ser)
 gnomAD v3 gnomAD v4
20g.61928298A>TCA317137577CDH4c.1880A>T (p.Asn627Ile)
c.1658A>T (p.Asn553Ile)
c.1598A>T (p.Asn533Ile)
c.1769A>T (p.Asn590Ile)
 dbSNP
20g.61928299C>ACA409509023CDH4c.1881C>A (p.Asn627Lys)
c.1659C>A (p.Asn553Lys)
c.1599C>A (p.Asn533Lys)
c.1770C>A (p.Asn590Lys)
20g.61928299C>GCA409509025CDH4c.1881C>G (p.Asn627Lys)
c.1659C>G (p.Asn553Lys)
c.1599C>G (p.Asn533Lys)
c.1770C>G (p.Asn590Lys)
20g.61928299C>TCA511322200CDH4c.1881C>T (p.Asn627=)
c.1659C>T (p.Asn553=)
c.1599C>T (p.Asn533=)
c.1770C>T (p.Asn590=)
 gnomAD v4
20g.61928300C>ACA409509027CDH4c.1882C>A (p.Leu628Met)
c.1660C>A (p.Leu554Met)
c.1600C>A (p.Leu534Met)
c.1771C>A (p.Leu591Met)
20g.61928300C>GCA409509028CDH4c.1882C>G (p.Leu628Val)
c.1660C>G (p.Leu554Val)
c.1600C>G (p.Leu534Val)
c.1771C>G (p.Leu591Val)
20g.61928300C>TCA511322202CDH4c.1882C>T (p.Leu628=)
c.1660C>T (p.Leu554=)
c.1600C>T (p.Leu534=)
c.1771C>T (p.Leu591=)
20g.61928301T>ACA409509031CDH4c.1883T>A (p.Leu628Gln)
c.1661T>A (p.Leu554Gln)
c.1601T>A (p.Leu534Gln)
c.1772T>A (p.Leu591Gln)
20g.61928301T>CCA409509033CDH4c.1883T>C (p.Leu628Pro)
c.1661T>C (p.Leu554Pro)
c.1601T>C (p.Leu534Pro)
c.1772T>C (p.Leu591Pro)
 dbSNP gnomAD v2 gnomAD v4
20g.61928301T>GCA409509034CDH4c.1883T>G (p.Leu628Arg)
c.1661T>G (p.Leu554Arg)
c.1601T>G (p.Leu534Arg)
c.1772T>G (p.Leu591Arg)
20g.61928301T=CA2373989249CDH4c.1883T= (p.Leu628=)
c.1661T= (p.Leu554=)
c.1601T= (p.Leu534=)
c.1772T= (p.Leu591=)
20g.61928302G>ACA511322204CDH4c.1884G>A (p.Leu628=)
c.1662G>A (p.Leu554=)
c.1602G>A (p.Leu534=)
c.1773G>A (p.Leu591=)
 dbSNP
20g.61928302G>CCA511322205CDH4c.1884G>C (p.Leu628=)
c.1662G>C (p.Leu554=)
c.1602G>C (p.Leu534=)
c.1773G>C (p.Leu591=)
20g.61928302G=CA2373989250CDH4c.1884G= (p.Leu628=)
c.1662G= (p.Leu554=)
c.1602G= (p.Leu534=)
c.1773G= (p.Leu591=)
20g.61928302G>TCA511322207CDH4c.1884G>T (p.Leu628=)
c.1662G>T (p.Leu554=)
c.1602G>T (p.Leu534=)
c.1773G>T (p.Leu591=)
 gnomAD v4
20g.61928303A>CCA409509040CDH4c.1885A>C (p.Asn629His)
c.1663A>C (p.Asn555His)
c.1603A>C (p.Asn535His)
c.1774A>C (p.Asn592His)
20g.61928303A>GCA409509039CDH4c.1885A>G (p.Asn629Asp)
c.1663A>G (p.Asn555Asp)
c.1603A>G (p.Asn535Asp)
c.1774A>G (p.Asn592Asp)
20g.61928303A>TCA409509037CDH4c.1885A>T (p.Asn629Tyr)
c.1663A>T (p.Asn555Tyr)
c.1603A>T (p.Asn535Tyr)
c.1774A>T (p.Asn592Tyr)
20g.61928304A>CCA409509044CDH4c.1886A>C (p.Asn629Thr)
c.1664A>C (p.Asn555Thr)
c.1604A>C (p.Asn535Thr)
c.1775A>C (p.Asn592Thr)
20g.61928304A>GCA409509045CDH4c.1886A>G (p.Asn629Ser)
c.1664A>G (p.Asn555Ser)
c.1604A>G (p.Asn535Ser)
c.1775A>G (p.Asn592Ser)
20g.61928304A>TCA409509047CDH4c.1886A>T (p.Asn629Ile)
c.1664A>T (p.Asn555Ile)
c.1604A>T (p.Asn535Ile)
c.1775A>T (p.Asn592Ile)
20g.61928305C>ACA409509050CDH4c.1887C>A (p.Asn629Lys)
c.1665C>A (p.Asn555Lys)
c.1605C>A (p.Asn535Lys)
c.1776C>A (p.Asn592Lys)
20g.61928305C=CA2373989251CDH4c.1887C= (p.Asn629=)
c.1665C= (p.Asn555=)
c.1605C= (p.Asn535=)
c.1776C= (p.Asn592=)
20g.61928305C>GCA409509051CDH4c.1887C>G (p.Asn629Lys)
c.1665C>G (p.Asn555Lys)
c.1605C>G (p.Asn535Lys)
c.1776C>G (p.Asn592Lys)
20g.61928305C>TCA9934894CDH4c.1887C>T (p.Asn629=)
c.1665C>T (p.Asn555=)
c.1605C>T (p.Asn535=)
c.1776C>T (p.Asn592=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928306G>ACA9934896CDH4c.1888G>A (p.Ala630Thr)
c.1666G>A (p.Ala556Thr)
c.1606G>A (p.Ala536Thr)
c.1777G>A (p.Ala593Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928306G>CCA409509057CDH4c.1888G>C (p.Ala630Pro)
c.1666G>C (p.Ala556Pro)
c.1606G>C (p.Ala536Pro)
c.1777G>C (p.Ala593Pro)
20g.61928306G=CA2373989252CDH4c.1888G= (p.Ala630=)
c.1666G= (p.Ala556=)
c.1606G= (p.Ala536=)
c.1777G= (p.Ala593=)
20g.61928306G>TCA9934895CDH4c.1888G>T (p.Ala630Ser)
c.1666G>T (p.Ala556Ser)
c.1606G>T (p.Ala536Ser)
c.1777G>T (p.Ala593Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928307C>ACA409509060CDH4c.1889C>A (p.Ala630Asp)
c.1667C>A (p.Ala556Asp)
c.1607C>A (p.Ala536Asp)
c.1778C>A (p.Ala593Asp)
20g.61928307C=CA2373989253CDH4c.1889C= (p.Ala630=)
c.1667C= (p.Ala556=)
c.1607C= (p.Ala536=)
c.1778C= (p.Ala593=)
20g.61928307C>GCA409509062CDH4c.1889C>G (p.Ala630Gly)
c.1667C>G (p.Ala556Gly)
c.1607C>G (p.Ala536Gly)
c.1778C>G (p.Ala593Gly)
20g.61928307C>TCA317137628CDH4c.1889C>T (p.Ala630Val)
c.1667C>T (p.Ala556Val)
c.1607C>T (p.Ala536Val)
c.1778C>T (p.Ala593Val)
 dbSNP gnomAD v3 gnomAD v4
20g.61928308C>ACA511322212CDH4c.1890C>A (p.Ala630=)
c.1668C>A (p.Ala556=)
c.1608C>A (p.Ala536=)
c.1779C>A (p.Ala593=)
20g.61928308C>GCA511322214CDH4c.1890C>G (p.Ala630=)
c.1668C>G (p.Ala556=)
c.1608C>G (p.Ala536=)
c.1779C>G (p.Ala593=)
20g.61928308C>TCA511322211CDH4c.1890C>T (p.Ala630=)
c.1668C>T (p.Ala556=)
c.1608C>T (p.Ala536=)
c.1779C>T (p.Ala593=)
 gnomAD v4
20g.61928309A=CA2373989254CDH4c.1891A= (p.Ile631=)
c.1669A= (p.Ile557=)
c.1609A= (p.Ile537=)
c.1780A= (p.Ile594=)
20g.61928309A>CCA409509065CDH4c.1891A>C (p.Ile631Leu)
c.1669A>C (p.Ile557Leu)
c.1609A>C (p.Ile537Leu)
c.1780A>C (p.Ile594Leu)
20g.61928309A>GCA409509066CDH4c.1891A>G (p.Ile631Val)
c.1669A>G (p.Ile557Val)
c.1609A>G (p.Ile537Val)
c.1780A>G (p.Ile594Val)
 dbSNP gnomAD v2 gnomAD v4
20g.61928309A>TCA409509068CDH4c.1891A>T (p.Ile631Phe)
c.1669A>T (p.Ile557Phe)
c.1609A>T (p.Ile537Phe)
c.1780A>T (p.Ile594Phe)
20g.61928310T>ACA409509071CDH4c.1892T>A (p.Ile631Asn)
c.1670T>A (p.Ile557Asn)
c.1610T>A (p.Ile537Asn)
c.1781T>A (p.Ile594Asn)
20g.61928310T>CCA409509074CDH4c.1892T>C (p.Ile631Thr)
c.1670T>C (p.Ile557Thr)
c.1610T>C (p.Ile537Thr)
c.1781T>C (p.Ile594Thr)
 dbSNP
20g.61928310T>GCA409509072CDH4c.1892T>G (p.Ile631Ser)
c.1670T>G (p.Ile557Ser)
c.1610T>G (p.Ile537Ser)
c.1781T>G (p.Ile594Ser)
20g.61928310T=CA2373989255CDH4c.1892T= (p.Ile631=)
c.1670T= (p.Ile557=)
c.1610T= (p.Ile537=)
c.1781T= (p.Ile594=)
20g.61928311C>ACA511322216CDH4c.1893C>A (p.Ile631=)
c.1671C>A (p.Ile557=)
c.1611C>A (p.Ile537=)
c.1782C>A (p.Ile594=)
20g.61928311C>GCA409509077CDH4c.1893C>G (p.Ile631Met)
c.1671C>G (p.Ile557Met)
c.1611C>G (p.Ile537Met)
c.1782C>G (p.Ile594Met)
20g.61928311C>TCA511322215CDH4c.1893C>T (p.Ile631=)
c.1671C>T (p.Ile557=)
c.1611C>T (p.Ile537=)
c.1782C>T (p.Ile594=)
20g.61928312A>CCA409509079CDH4c.1894A>C (p.Asn632His)
c.1672A>C (p.Asn558His)
c.1612A>C (p.Asn538His)
c.1783A>C (p.Asn595His)
20g.61928312A>GCA409509081CDH4c.1894A>G (p.Asn632Asp)
c.1672A>G (p.Asn558Asp)
c.1612A>G (p.Asn538Asp)
c.1783A>G (p.Asn595Asp)
20g.61928312A>TCA409509083CDH4c.1894A>T (p.Asn632Tyr)
c.1672A>T (p.Asn558Tyr)
c.1612A>T (p.Asn538Tyr)
c.1783A>T (p.Asn595Tyr)
20g.61928313A>CCA409509085CDH4c.1895A>C (p.Asn632Thr)
c.1673A>C (p.Asn558Thr)
c.1613A>C (p.Asn538Thr)
c.1784A>C (p.Asn595Thr)
20g.61928313A>GCA409509087CDH4c.1895A>G (p.Asn632Ser)
c.1673A>G (p.Asn558Ser)
c.1613A>G (p.Asn538Ser)
c.1784A>G (p.Asn595Ser)
20g.61928313A>TCA409509089CDH4c.1895A>T (p.Asn632Ile)
c.1673A>T (p.Asn558Ile)
c.1613A>T (p.Asn538Ile)
c.1784A>T (p.Asn595Ile)
20g.61928314C>ACA409509091CDH4c.1896C>A (p.Asn632Lys)
c.1674C>A (p.Asn558Lys)
c.1614C>A (p.Asn538Lys)
c.1785C>A (p.Asn595Lys)
20g.61928314C=CA2373989256CDH4c.1896C= (p.Asn632=)
c.1674C= (p.Asn558=)
c.1614C= (p.Asn538=)
c.1785C= (p.Asn595=)
20g.61928314C>GCA409509093CDH4c.1896C>G (p.Asn632Lys)
c.1674C>G (p.Asn558Lys)
c.1614C>G (p.Asn538Lys)
c.1785C>G (p.Asn595Lys)
20g.61928314C>TCA511322217CDH4c.1896C>T (p.Asn632=)
c.1674C>T (p.Asn558=)
c.1614C>T (p.Asn538=)
c.1785C>T (p.Asn595=)
 dbSNP gnomAD v2 gnomAD v4
20g.61928315A=CA2373989257CDH4c.1897A= (p.Ile633=)
c.1675A= (p.Ile559=)
c.1615A= (p.Ile539=)
c.1786A= (p.Ile596=)
20g.61928315A>CCA409509095CDH4c.1897A>C (p.Ile633Leu)
c.1675A>C (p.Ile559Leu)
c.1615A>C (p.Ile539Leu)
c.1786A>C (p.Ile596Leu)
20g.61928315A>GCA9934897CDH4c.1897A>G (p.Ile633Val)
c.1675A>G (p.Ile559Val)
c.1615A>G (p.Ile539Val)
c.1786A>G (p.Ile596Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928315A>TCA409509098CDH4c.1897A>T (p.Ile633Phe)
c.1675A>T (p.Ile559Phe)
c.1615A>T (p.Ile539Phe)
c.1786A>T (p.Ile596Phe)
20g.61928316T>ACA409509102CDH4c.1898T>A (p.Ile633Asn)
c.1676T>A (p.Ile559Asn)
c.1616T>A (p.Ile539Asn)
c.1787T>A (p.Ile596Asn)
20g.61928316T>CCA409509104CDH4c.1898T>C (p.Ile633Thr)
c.1676T>C (p.Ile559Thr)
c.1616T>C (p.Ile539Thr)
c.1787T>C (p.Ile596Thr)
 dbSNP gnomAD v3 gnomAD v4
20g.61928316T>GCA409509100CDH4c.1898T>G (p.Ile633Ser)
c.1676T>G (p.Ile559Ser)
c.1616T>G (p.Ile539Ser)
c.1787T>G (p.Ile596Ser)
20g.61928316T=CA2373989258CDH4c.1898T= (p.Ile633=)
c.1676T= (p.Ile559=)
c.1616T= (p.Ile539=)
c.1787T= (p.Ile596=)
20g.61928317C>ACA511322221CDH4c.1899C>A (p.Ile633=)
c.1677C>A (p.Ile559=)
c.1617C>A (p.Ile539=)
c.1788C>A (p.Ile596=)
20g.61928317C=CA2373989259CDH4c.1899C= (p.Ile633=)
c.1677C= (p.Ile559=)
c.1617C= (p.Ile539=)
c.1788C= (p.Ile596=)
20g.61928317C>GCA409509106CDH4c.1899C>G (p.Ile633Met)
c.1677C>G (p.Ile559Met)
c.1617C>G (p.Ile539Met)
c.1788C>G (p.Ile596Met)
20g.61928317C>TCA9934898CDH4c.1899C>T (p.Ile633=)
c.1677C>T (p.Ile559=)
c.1617C>T (p.Ile539=)
c.1788C>T (p.Ile596=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928318A>CCA409509109CDH4c.1900A>C (p.Thr634Pro)
c.1678A>C (p.Thr560Pro)
c.1618A>C (p.Thr540Pro)
c.1789A>C (p.Thr597Pro)
20g.61928318A>GCA409509110CDH4c.1900A>G (p.Thr634Ala)
c.1678A>G (p.Thr560Ala)
c.1618A>G (p.Thr540Ala)
c.1789A>G (p.Thr597Ala)
20g.61928318A>TCA409509112CDH4c.1900A>T (p.Thr634Ser)
c.1678A>T (p.Thr560Ser)
c.1618A>T (p.Thr540Ser)
c.1789A>T (p.Thr597Ser)
20g.61928319C>ACA317137631CDH4c.1901C>A (p.Thr634Lys)
c.1679C>A (p.Thr560Lys)
c.1619C>A (p.Thr540Lys)
c.1790C>A (p.Thr597Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928319C=CA2373989260CDH4c.1901C= (p.Thr634=)
c.1679C= (p.Thr560=)
c.1619C= (p.Thr540=)
c.1790C= (p.Thr597=)
20g.61928319C>GCA409509115CDH4c.1901C>G (p.Thr634Arg)
c.1679C>G (p.Thr560Arg)
c.1619C>G (p.Thr540Arg)
c.1790C>G (p.Thr597Arg)
 gnomAD v4
20g.61928319C>TCA9934899CDH4c.1901C>T (p.Thr634Met)
c.1679C>T (p.Thr560Met)
c.1619C>T (p.Thr540Met)
c.1790C>T (p.Thr597Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928320G>ACA9934900CDH4c.1902G>A (p.Thr634=)
c.1680G>A (p.Thr560=)
c.1620G>A (p.Thr540=)
c.1791G>A (p.Thr597=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928320G>CCA511322224CDH4c.1902G>C (p.Thr634=)
c.1680G>C (p.Thr560=)
c.1620G>C (p.Thr540=)
c.1791G>C (p.Thr597=)
 dbSNP
20g.61928320G=CA2373989261CDH4c.1902G= (p.Thr634=)
c.1680G= (p.Thr560=)
c.1620G= (p.Thr540=)
c.1791G= (p.Thr597=)
20g.61928320G>TCA511322226CDH4c.1902G>T (p.Thr634=)
c.1680G>T (p.Thr560=)
c.1620G>T (p.Thr540=)
c.1791G>T (p.Thr597=)
 gnomAD v4
20g.61928321G>ACA409509119CDH4c.1903G>A (p.Ala635Thr)
c.1681G>A (p.Ala561Thr)
c.1621G>A (p.Ala541Thr)
c.1792G>A (p.Ala598Thr)
 dbSNP gnomAD v2
20g.61928321G>CCA409509121CDH4c.1903G>C (p.Ala635Pro)
c.1681G>C (p.Ala561Pro)
c.1621G>C (p.Ala541Pro)
c.1792G>C (p.Ala598Pro)
20g.61928321G=CA2373989262CDH4c.1903G= (p.Ala635=)
c.1681G= (p.Ala561=)
c.1621G= (p.Ala541=)
c.1792G= (p.Ala598=)
20g.61928321G>TCA409509123CDH4c.1903G>T (p.Ala635Ser)
c.1681G>T (p.Ala561Ser)
c.1621G>T (p.Ala541Ser)
c.1792G>T (p.Ala598Ser)
 gnomAD v4
20g.61928322C>ACA409509126CDH4c.1904C>A (p.Ala635Glu)
c.1682C>A (p.Ala561Glu)
c.1622C>A (p.Ala541Glu)
c.1793C>A (p.Ala598Glu)
20g.61928322C=CA2373989263CDH4c.1904C= (p.Ala635=)
c.1682C= (p.Ala561=)
c.1622C= (p.Ala541=)
c.1793C= (p.Ala598=)
20g.61928322C>GCA409509127CDH4c.1904C>G (p.Ala635Gly)
c.1682C>G (p.Ala561Gly)
c.1622C>G (p.Ala541Gly)
c.1793C>G (p.Ala598Gly)
20g.61928322C>TCA9934901CDH4c.1904C>T (p.Ala635Val)
c.1682C>T (p.Ala561Val)
c.1622C>T (p.Ala541Val)
c.1793C>T (p.Ala598Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928323G>ACA317137658CDH4c.1905G>A (p.Ala635=)
c.1683G>A (p.Ala561=)
c.1623G>A (p.Ala541=)
c.1794G>A (p.Ala598=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928323G>CCA511322228CDH4c.1905G>C (p.Ala635=)
c.1683G>C (p.Ala561=)
c.1623G>C (p.Ala541=)
c.1794G>C (p.Ala598=)
 gnomAD v4
20g.61928323G=CA2373989264CDH4c.1905G= (p.Ala635=)
c.1683G= (p.Ala561=)
c.1623G= (p.Ala541=)
c.1794G= (p.Ala598=)
20g.61928323G>TCA511322229CDH4c.1905G>T (p.Ala635=)
c.1683G>T (p.Ala561=)
c.1623G>T (p.Ala541=)
c.1794G>T (p.Ala598=)
 gnomAD v4
20g.61928324delCA913079321CDH4c.1906del (p.Ala636ProfsTer?)
c.1684del (p.Ala562ProfsTer?)
c.1624del (p.Ala542ProfsTer?)
c.1795del (p.Ala599ProfsTer?)
20g.61928324G>ACA409509134CDH4c.1906G>A (p.Ala636Thr)
c.1684G>A (p.Ala562Thr)
c.1624G>A (p.Ala542Thr)
c.1795G>A (p.Ala599Thr)
20g.61928324G>CCA409509131CDH4c.1906G>C (p.Ala636Pro)
c.1684G>C (p.Ala562Pro)
c.1624G>C (p.Ala542Pro)
c.1795G>C (p.Ala599Pro)
20g.61928324G>TCA409509132CDH4c.1906G>T (p.Ala636Ser)
c.1684G>T (p.Ala562Ser)
c.1624G>T (p.Ala542Ser)
c.1795G>T (p.Ala599Ser)
 gnomAD v4
20g.61928325C>ACA409509137CDH4c.1907C>A (p.Ala636Asp)
c.1685C>A (p.Ala562Asp)
c.1625C>A (p.Ala542Asp)
c.1796C>A (p.Ala599Asp)
20g.61928325C>GCA409509138CDH4c.1907C>G (p.Ala636Gly)
c.1685C>G (p.Ala562Gly)
c.1625C>G (p.Ala542Gly)
c.1796C>G (p.Ala599Gly)
 dbSNP
20g.61928325C>TCA409509140CDH4c.1907C>T (p.Ala636Val)
c.1685C>T (p.Ala562Val)
c.1625C>T (p.Ala542Val)
c.1796C>T (p.Ala599Val)
 gnomAD v4 COSMIC
20g.61928326C>ACA511322231CDH4c.1908C>A (p.Ala636=)
c.1686C>A (p.Ala562=)
c.1626C>A (p.Ala542=)
c.1797C>A (p.Ala599=)
20g.61928326C=CA2373989265CDH4c.1908C= (p.Ala636=)
c.1686C= (p.Ala562=)
c.1626C= (p.Ala542=)
c.1797C= (p.Ala599=)
20g.61928326C>GCA511322232CDH4c.1908C>G (p.Ala636=)
c.1686C>G (p.Ala562=)
c.1626C>G (p.Ala542=)
c.1797C>G (p.Ala599=)
20g.61928326C>TCA9934902CDH4c.1908C>T (p.Ala636=)
c.1686C>T (p.Ala562=)
c.1626C>T (p.Ala542=)
c.1797C>T (p.Ala599=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928327G>ACA409509143CDH4c.1909G>A (p.Asp637Asn)
c.1687G>A (p.Asp563Asn)
c.1627G>A (p.Asp543Asn)
c.1798G>A (p.Asp600Asn)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928327G>CCA409509145CDH4c.1909G>C (p.Asp637His)
c.1687G>C (p.Asp563His)
c.1627G>C (p.Asp543His)
c.1798G>C (p.Asp600His)
20g.61928327G=CA2373989266CDH4c.1909G= (p.Asp637=)
c.1687G= (p.Asp563=)
c.1627G= (p.Asp543=)
c.1798G= (p.Asp600=)
20g.61928327G>TCA409509147CDH4c.1909G>T (p.Asp637Tyr)
c.1687G>T (p.Asp563Tyr)
c.1627G>T (p.Asp543Tyr)
c.1798G>T (p.Asp600Tyr)
 gnomAD v4
20g.61928328A>CCA409509149CDH4c.1910A>C (p.Asp637Ala)
c.1688A>C (p.Asp563Ala)
c.1628A>C (p.Asp543Ala)
c.1799A>C (p.Asp600Ala)
20g.61928328A>GCA409509151CDH4c.1910A>G (p.Asp637Gly)
c.1688A>G (p.Asp563Gly)
c.1628A>G (p.Asp543Gly)
c.1799A>G (p.Asp600Gly)
 dbSNP
20g.61928328A>TCA409509153CDH4c.1910A>T (p.Asp637Val)
c.1688A>T (p.Asp563Val)
c.1628A>T (p.Asp543Val)
c.1799A>T (p.Asp600Val)
20g.61928329C>ACA409509154CDH4c.1911C>A (p.Asp637Glu)
c.1689C>A (p.Asp563Glu)
c.1629C>A (p.Asp543Glu)
c.1800C>A (p.Asp600Glu)
20g.61928329C=CA2373989267CDH4c.1911C= (p.Asp637=)
c.1689C= (p.Asp563=)
c.1629C= (p.Asp543=)
c.1800C= (p.Asp600=)
20g.61928329C>GCA409509156CDH4c.1911C>G (p.Asp637Glu)
c.1689C>G (p.Asp563Glu)
c.1629C>G (p.Asp543Glu)
c.1800C>G (p.Asp600Glu)
20g.61928329C>TCA9934903CDH4c.1911C>T (p.Asp637=)
c.1689C>T (p.Asp563=)
c.1629C>T (p.Asp543=)
c.1800C>T (p.Asp600=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928330G>ACA317137663CDH4c.1912G>A (p.Ala638Thr)
c.1690G>A (p.Ala564Thr)
c.1630G>A (p.Ala544Thr)
c.1801G>A (p.Ala601Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928330G>CCA409509159CDH4c.1912G>C (p.Ala638Pro)
c.1690G>C (p.Ala564Pro)
c.1630G>C (p.Ala544Pro)
c.1801G>C (p.Ala601Pro)
20g.61928330G=CA2373989268CDH4c.1912G= (p.Ala638=)
c.1690G= (p.Ala564=)
c.1630G= (p.Ala544=)
c.1801G= (p.Ala601=)
20g.61928330G>TCA409509161CDH4c.1912G>T (p.Ala638Ser)
c.1690G>T (p.Ala564Ser)
c.1630G>T (p.Ala544Ser)
c.1801G>T (p.Ala601Ser)
 gnomAD v4
20g.61928331C>ACA409509164CDH4c.1913C>A (p.Ala638Asp)
c.1691C>A (p.Ala564Asp)
c.1631C>A (p.Ala544Asp)
c.1802C>A (p.Ala601Asp)
20g.61928331C=CA2373989269CDH4c.1913C= (p.Ala638=)
c.1691C= (p.Ala564=)
c.1631C= (p.Ala544=)
c.1802C= (p.Ala601=)
20g.61928331C>GCA409509165CDH4c.1913C>G (p.Ala638Gly)
c.1691C>G (p.Ala564Gly)
c.1631C>G (p.Ala544Gly)
c.1802C>G (p.Ala601Gly)
 gnomAD v4
20g.61928331C>TCA409509167CDH4c.1913C>T (p.Ala638Val)
c.1691C>T (p.Ala564Val)
c.1631C>T (p.Ala544Val)
c.1802C>T (p.Ala601Val)
 dbSNP gnomAD v2 gnomAD v4
20g.61928332T>ACA511322237CDH4c.1914T>A (p.Ala638=)
c.1692T>A (p.Ala564=)
c.1632T>A (p.Ala544=)
c.1803T>A (p.Ala601=)
20g.61928332T>CCA317137670CDH4c.1914T>C (p.Ala638=)
c.1692T>C (p.Ala564=)
c.1632T>C (p.Ala544=)
c.1803T>C (p.Ala601=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928332T>GCA511322238CDH4c.1914T>G (p.Ala638=)
c.1692T>G (p.Ala564=)
c.1632T>G (p.Ala544=)
c.1803T>G (p.Ala601=)
20g.61928332T=CA2373989270CDH4c.1914T= (p.Ala638=)
c.1692T= (p.Ala564=)
c.1632T= (p.Ala544=)
c.1803T= (p.Ala601=)
20g.61928333G>ACA409509169CDH4c.1915G>A (p.Asp639Asn)
c.1693G>A (p.Asp565Asn)
c.1633G>A (p.Asp545Asn)
c.1804G>A (p.Asp602Asn)
20g.61928333G>CCA409509170CDH4c.1915G>C (p.Asp639His)
c.1693G>C (p.Asp565His)
c.1633G>C (p.Asp545His)
c.1804G>C (p.Asp602His)
20g.61928333G>TCA409509172CDH4c.1915G>T (p.Asp639Tyr)
c.1693G>T (p.Asp565Tyr)
c.1633G>T (p.Asp545Tyr)
c.1804G>T (p.Asp602Tyr)
20g.61928334A>CCA409509174CDH4c.1916A>C (p.Asp639Ala)
c.1694A>C (p.Asp565Ala)
c.1634A>C (p.Asp545Ala)
c.1805A>C (p.Asp602Ala)
20g.61928334A>GCA409509176CDH4c.1916A>G (p.Asp639Gly)
c.1694A>G (p.Asp565Gly)
c.1634A>G (p.Asp545Gly)
c.1805A>G (p.Asp602Gly)
 gnomAD v4
20g.61928334A>TCA409509178CDH4c.1916A>T (p.Asp639Val)
c.1694A>T (p.Asp565Val)
c.1634A>T (p.Asp545Val)
c.1805A>T (p.Asp602Val)
20g.61928335C>ACA409509180CDH4c.1917C>A (p.Asp639Glu)
c.1695C>A (p.Asp565Glu)
c.1635C>A (p.Asp545Glu)
c.1806C>A (p.Asp602Glu)
20g.61928335C=CA2373989271CDH4c.1917C= (p.Asp639=)
c.1695C= (p.Asp565=)
c.1635C= (p.Asp545=)
c.1806C= (p.Asp602=)
20g.61928335C>GCA409509182CDH4c.1917C>G (p.Asp639Glu)
c.1695C>G (p.Asp565Glu)
c.1635C>G (p.Asp545Glu)
c.1806C>G (p.Asp602Glu)
20g.61928335C>TCA9934904CDH4c.1917C>T (p.Asp639=)
c.1695C>T (p.Asp565=)
c.1635C>T (p.Asp545=)
c.1806C>T (p.Asp602=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928336G>ACA9934905CDH4c.1918G>A (p.Val640Ile)
c.1696G>A (p.Val566Ile)
c.1636G>A (p.Val546Ile)
c.1807G>A (p.Val603Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928336G>CCA409509187CDH4c.1918G>C (p.Val640Leu)
c.1696G>C (p.Val566Leu)
c.1636G>C (p.Val546Leu)
c.1807G>C (p.Val603Leu)
20g.61928336G=CA2373989272CDH4c.1918G= (p.Val640=)
c.1696G= (p.Val566=)
c.1636G= (p.Val546=)
c.1807G= (p.Val603=)
20g.61928336G>TCA409509185CDH4c.1918G>T (p.Val640Phe)
c.1696G>T (p.Val566Phe)
c.1636G>T (p.Val546Phe)
c.1807G>T (p.Val603Phe)
20g.61928337T>ACA409509190CDH4c.1919T>A (p.Val640Asp)
c.1697T>A (p.Val566Asp)
c.1637T>A (p.Val546Asp)
c.1808T>A (p.Val603Asp)
20g.61928337T>CCA409509192CDH4c.1919T>C (p.Val640Ala)
c.1697T>C (p.Val566Ala)
c.1637T>C (p.Val546Ala)
c.1808T>C (p.Val603Ala)
20g.61928337T>GCA409509194CDH4c.1919T>G (p.Val640Gly)
c.1697T>G (p.Val566Gly)
c.1637T>G (p.Val546Gly)
c.1808T>G (p.Val603Gly)
20g.61928338C>ACA511322242CDH4c.1920C>A (p.Val640=)
c.1698C>A (p.Val566=)
c.1638C>A (p.Val546=)
c.1809C>A (p.Val603=)
20g.61928338C=CA2373989273CDH4c.1920C= (p.Val640=)
c.1698C= (p.Val566=)
c.1638C= (p.Val546=)
c.1809C= (p.Val603=)
20g.61928338C>GCA511322244CDH4c.1920C>G (p.Val640=)
c.1698C>G (p.Val566=)
c.1638C>G (p.Val546=)
c.1809C>G (p.Val603=)
20g.61928338C>TCA9934906CDH4c.1920C>T (p.Val640=)
c.1698C>T (p.Val566=)
c.1638C>T (p.Val546=)
c.1809C>T (p.Val603=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928339G>ACA9934907CDH4c.1921G>A (p.Asp641Asn)
c.1699G>A (p.Asp567Asn)
c.1639G>A (p.Asp547Asn)
c.1810G>A (p.Asp604Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928339G>CCA409509199CDH4c.1921G>C (p.Asp641His)
c.1699G>C (p.Asp567His)
c.1639G>C (p.Asp547His)
c.1810G>C (p.Asp604His)
 dbSNP
20g.61928339G=CA2373989274CDH4c.1921G= (p.Asp641=)
c.1699G= (p.Asp567=)
c.1639G= (p.Asp547=)
c.1810G= (p.Asp604=)
20g.61928339G>TCA409509200CDH4c.1921G>T (p.Asp641Tyr)
c.1699G>T (p.Asp567Tyr)
c.1639G>T (p.Asp547Tyr)
c.1810G>T (p.Asp604Tyr)
20g.61928340A>CCA409509202CDH4c.1922A>C (p.Asp641Ala)
c.1700A>C (p.Asp567Ala)
c.1640A>C (p.Asp547Ala)
c.1811A>C (p.Asp604Ala)
20g.61928340A>GCA409509205CDH4c.1922A>G (p.Asp641Gly)
c.1700A>G (p.Asp567Gly)
c.1640A>G (p.Asp547Gly)
c.1811A>G (p.Asp604Gly)
20g.61928340A>TCA409509206CDH4c.1922A>T (p.Asp641Val)
c.1700A>T (p.Asp567Val)
c.1640A>T (p.Asp547Val)
c.1811A>T (p.Asp604Val)
20g.61928341C>ACA409509209CDH4c.1923C>A (p.Asp641Glu)
c.1701C>A (p.Asp567Glu)
c.1641C>A (p.Asp547Glu)
c.1812C>A (p.Asp604Glu)
20g.61928341C=CA2373989275CDH4c.1923C= (p.Asp641=)
c.1701C= (p.Asp567=)
c.1641C= (p.Asp547=)
c.1812C= (p.Asp604=)
20g.61928341C>GCA9934908CDH4c.1923C>G (p.Asp641Glu)
c.1701C>G (p.Asp567Glu)
c.1641C>G (p.Asp547Glu)
c.1812C>G (p.Asp604Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928341C>TCA317137715CDH4c.1923C>T (p.Asp641=)
c.1701C>T (p.Asp567=)
c.1641C>T (p.Asp547=)
c.1812C>T (p.Asp604=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928342C>ACA409509215CDH4c.1924C>A (p.Pro642Thr)
c.1702C>A (p.Pro568Thr)
c.1642C>A (p.Pro548Thr)
c.1813C>A (p.Pro605Thr)
20g.61928342C>GCA409509217CDH4c.1924C>G (p.Pro642Ala)
c.1702C>G (p.Pro568Ala)
c.1642C>G (p.Pro548Ala)
c.1813C>G (p.Pro605Ala)
 gnomAD v4
20g.61928342C>TCA409509212CDH4c.1924C>T (p.Pro642Ser)
c.1702C>T (p.Pro568Ser)
c.1642C>T (p.Pro548Ser)
c.1813C>T (p.Pro605Ser)
 COSMIC
20g.61928343C>ACA409509219CDH4c.1925C>A (p.Pro642His)
c.1703C>A (p.Pro568His)
c.1643C>A (p.Pro548His)
c.1814C>A (p.Pro605His)
20g.61928343C>GCA409509222CDH4c.1925C>G (p.Pro642Arg)
c.1703C>G (p.Pro568Arg)
c.1643C>G (p.Pro548Arg)
c.1814C>G (p.Pro605Arg)
20g.61928343C>TCA409509221CDH4c.1925C>T (p.Pro642Leu)
c.1703C>T (p.Pro568Leu)
c.1643C>T (p.Pro548Leu)
c.1814C>T (p.Pro605Leu)
20g.61928344C>ACA511322247CDH4c.1926C>A (p.Pro642=)
c.1704C>A (p.Pro568=)
c.1644C>A (p.Pro548=)
c.1815C>A (p.Pro605=)
20g.61928344C=CA2373989276CDH4c.1926C= (p.Pro642=)
c.1704C= (p.Pro568=)
c.1644C= (p.Pro548=)
c.1815C= (p.Pro605=)
20g.61928344C>GCA511322249CDH4c.1926C>G (p.Pro642=)
c.1704C>G (p.Pro568=)
c.1644C>G (p.Pro548=)
c.1815C>G (p.Pro605=)
20g.61928344C>TCA9934909CDH4c.1926C>T (p.Pro642=)
c.1704C>T (p.Pro568=)
c.1644C>T (p.Pro548=)
c.1815C>T (p.Pro605=)
 dbSNP ExAC gnomAD v2
20g.61928345A>CCA409509226CDH4c.1927A>C (p.Asn643His)
c.1705A>C (p.Asn569His)
c.1645A>C (p.Asn549His)
c.1816A>C (p.Asn606His)
20g.61928345A>GCA409509227CDH4c.1927A>G (p.Asn643Asp)
c.1705A>G (p.Asn569Asp)
c.1645A>G (p.Asn549Asp)
c.1816A>G (p.Asn606Asp)
20g.61928345A>TCA409509229CDH4c.1927A>T (p.Asn643Tyr)
c.1705A>T (p.Asn569Tyr)
c.1645A>T (p.Asn549Tyr)
c.1816A>T (p.Asn606Tyr)
20g.61928346A=CA2373989277CDH4c.1928A= (p.Asn643=)
c.1706A= (p.Asn569=)
c.1646A= (p.Asn549=)
c.1817A= (p.Asn606=)
20g.61928346A>CCA409509231CDH4c.1928A>C (p.Asn643Thr)
c.1706A>C (p.Asn569Thr)
c.1646A>C (p.Asn549Thr)
c.1817A>C (p.Asn606Thr)
20g.61928346A>GCA317137749CDH4c.1928A>G (p.Asn643Ser)
c.1706A>G (p.Asn569Ser)
c.1646A>G (p.Asn549Ser)
c.1817A>G (p.Asn606Ser)
 dbSNP gnomAD v2
20g.61928346A>TCA409509233CDH4c.1928A>T (p.Asn643Ile)
c.1706A>T (p.Asn569Ile)
c.1646A>T (p.Asn549Ile)
c.1817A>T (p.Asn606Ile)
20g.61928347C>ACA409509235CDH4c.1929C>A (p.Asn643Lys)
c.1707C>A (p.Asn569Lys)
c.1647C>A (p.Asn549Lys)
c.1818C>A (p.Asn606Lys)
20g.61928347C>GCA409509237CDH4c.1929C>G (p.Asn643Lys)
c.1707C>G (p.Asn569Lys)
c.1647C>G (p.Asn549Lys)
c.1818C>G (p.Asn606Lys)
20g.61928347C>TCA511322251CDH4c.1929C>T (p.Asn643=)
c.1707C>T (p.Asn569=)
c.1647C>T (p.Asn549=)
c.1818C>T (p.Asn606=)
 gnomAD v4
20g.61928348A>CCA409509239CDH4c.1930A>C (p.Ile644Leu)
c.1708A>C (p.Ile570Leu)
c.1648A>C (p.Ile550Leu)
c.1819A>C (p.Ile607Leu)
20g.61928348A>GCA409509241CDH4c.1930A>G (p.Ile644Val)
c.1708A>G (p.Ile570Val)
c.1648A>G (p.Ile550Val)
c.1819A>G (p.Ile607Val)
20g.61928348A>TCA409509243CDH4c.1930A>T (p.Ile644Phe)
c.1708A>T (p.Ile570Phe)
c.1648A>T (p.Ile550Phe)
c.1819A>T (p.Ile607Phe)
20g.61928349T>ACA409509248CDH4c.1931T>A (p.Ile644Asn)
c.1709T>A (p.Ile570Asn)
c.1649T>A (p.Ile550Asn)
c.1820T>A (p.Ile607Asn)
20g.61928349T>CCA409509245CDH4c.1931T>C (p.Ile644Thr)
c.1709T>C (p.Ile570Thr)
c.1649T>C (p.Ile550Thr)
c.1820T>C (p.Ile607Thr)
20g.61928349T>GCA409509247CDH4c.1931T>G (p.Ile644Ser)
c.1709T>G (p.Ile570Ser)
c.1649T>G (p.Ile550Ser)
c.1820T>G (p.Ile607Ser)
20g.61928350C>ACA511322253CDH4c.1932C>A (p.Ile644=)
c.1710C>A (p.Ile570=)
c.1650C>A (p.Ile550=)
c.1821C>A (p.Ile607=)
 gnomAD v4
20g.61928350C=CA2373989278CDH4c.1932C= (p.Ile644=)
c.1710C= (p.Ile570=)
c.1650C= (p.Ile550=)
c.1821C= (p.Ile607=)
20g.61928350C>GCA409509251CDH4c.1932C>G (p.Ile644Met)
c.1710C>G (p.Ile570Met)
c.1650C>G (p.Ile550Met)
c.1821C>G (p.Ile607Met)
20g.61928350C>TCA9934910CDH4c.1932C>T (p.Ile644=)
c.1710C>T (p.Ile570=)
c.1650C>T (p.Ile550=)
c.1821C>T (p.Ile607=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928351G>ACA9934911CDH4c.1933G>A (p.Gly645Ser)
c.1711G>A (p.Gly571Ser)
c.1651G>A (p.Gly551Ser)
c.1822G>A (p.Gly608Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928351G>CCA409509255CDH4c.1933G>C (p.Gly645Arg)
c.1711G>C (p.Gly571Arg)
c.1651G>C (p.Gly551Arg)
c.1822G>C (p.Gly608Arg)
20g.61928351G=CA2373989279CDH4c.1933G= (p.Gly645=)
c.1711G= (p.Gly571=)
c.1651G= (p.Gly551=)
c.1822G= (p.Gly608=)
20g.61928351G>TCA409509257CDH4c.1933G>T (p.Gly645Cys)
c.1711G>T (p.Gly571Cys)
c.1651G>T (p.Gly551Cys)
c.1822G>T (p.Gly608Cys)
 gnomAD v4
20g.61928352G>ACA409509258CDH4c.1934G>A (p.Gly645Asp)
c.1712G>A (p.Gly571Asp)
c.1652G>A (p.Gly551Asp)
c.1823G>A (p.Gly608Asp)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928352G>CCA409509260CDH4c.1934G>C (p.Gly645Ala)
c.1712G>C (p.Gly571Ala)
c.1652G>C (p.Gly551Ala)
c.1823G>C (p.Gly608Ala)
20g.61928352G=CA2373989280CDH4c.1934G= (p.Gly645=)
c.1712G= (p.Gly571=)
c.1652G= (p.Gly551=)
c.1823G= (p.Gly608=)
20g.61928352G>TCA9934912CDH4c.1934G>T (p.Gly645Val)
c.1712G>T (p.Gly571Val)
c.1652G>T (p.Gly551Val)
c.1823G>T (p.Gly608Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928353C>ACA511322256CDH4c.1935C>A (p.Gly645=)
c.1713C>A (p.Gly571=)
c.1653C>A (p.Gly551=)
c.1824C>A (p.Gly608=)
20g.61928353C=CA2373989281CDH4c.1935C= (p.Gly645=)
c.1713C= (p.Gly571=)
c.1653C= (p.Gly551=)
c.1824C= (p.Gly608=)
20g.61928353C>GCA511322254CDH4c.1935C>G (p.Gly645=)
c.1713C>G (p.Gly571=)
c.1653C>G (p.Gly551=)
c.1824C>G (p.Gly608=)
20g.61928353C>TCA511322255CDH4c.1935C>T (p.Gly645=)
c.1713C>T (p.Gly571=)
c.1653C>T (p.Gly551=)
c.1824C>T (p.Gly608=)
 dbSNP gnomAD v4
20g.61928354C>ACA409509262CDH4c.1936C>A (p.Pro646Thr)
c.1714C>A (p.Pro572Thr)
c.1654C>A (p.Pro552Thr)
c.1825C>A (p.Pro609Thr)
20g.61928354C>GCA409509264CDH4c.1936C>G (p.Pro646Ala)
c.1714C>G (p.Pro572Ala)
c.1654C>G (p.Pro552Ala)
c.1825C>G (p.Pro609Ala)
20g.61928354C>TCA409509266CDH4c.1936C>T (p.Pro646Ser)
c.1714C>T (p.Pro572Ser)
c.1654C>T (p.Pro552Ser)
c.1825C>T (p.Pro609Ser)
20g.61928355C>ACA409509272CDH4c.1937C>A (p.Pro646His)
c.1715C>A (p.Pro572His)
c.1655C>A (p.Pro552His)
c.1826C>A (p.Pro609His)
20g.61928355C=CA2373989282CDH4c.1937C= (p.Pro646=)
c.1715C= (p.Pro572=)
c.1655C= (p.Pro552=)
c.1826C= (p.Pro609=)
20g.61928355C>GCA9934913CDH4c.1937C>G (p.Pro646Arg)
c.1715C>G (p.Pro572Arg)
c.1655C>G (p.Pro552Arg)
c.1826C>G (p.Pro609Arg)
 dbSNP ExAC
20g.61928355C>TCA409509268CDH4c.1937C>T (p.Pro646Leu)
c.1715C>T (p.Pro572Leu)
c.1655C>T (p.Pro552Leu)
c.1826C>T (p.Pro609Leu)
20g.61928356C>ACA511322259CDH4c.1938C>A (p.Pro646=)
c.1716C>A (p.Pro572=)
c.1656C>A (p.Pro552=)
c.1827C>A (p.Pro609=)
20g.61928356C>GCA511322262CDH4c.1938C>G (p.Pro646=)
c.1716C>G (p.Pro572=)
c.1656C>G (p.Pro552=)
c.1827C>G (p.Pro609=)
20g.61928356C>TCA511322260CDH4c.1938C>T (p.Pro646=)
c.1716C>T (p.Pro572=)
c.1656C>T (p.Pro552=)
c.1827C>T (p.Pro609=)
20g.61928357T>ACA409509274CDH4c.1939T>A (p.Tyr647Asn)
c.1717T>A (p.Tyr573Asn)
c.1657T>A (p.Tyr553Asn)
c.1828T>A (p.Tyr610Asn)
20g.61928357T>CCA409509276CDH4c.1939T>C (p.Tyr647His)
c.1717T>C (p.Tyr573His)
c.1657T>C (p.Tyr553His)
c.1828T>C (p.Tyr610His)
20g.61928357T>GCA409509278CDH4c.1939T>G (p.Tyr647Asp)
c.1717T>G (p.Tyr573Asp)
c.1657T>G (p.Tyr553Asp)
c.1828T>G (p.Tyr610Asp)
20g.61928358A>CCA409509280CDH4c.1940A>C (p.Tyr647Ser)
c.1718A>C (p.Tyr573Ser)
c.1658A>C (p.Tyr553Ser)
c.1829A>C (p.Tyr610Ser)
20g.61928358A>GCA409509282CDH4c.1940A>G (p.Tyr647Cys)
c.1718A>G (p.Tyr573Cys)
c.1658A>G (p.Tyr553Cys)
c.1829A>G (p.Tyr610Cys)
20g.61928358A>TCA409509284CDH4c.1940A>T (p.Tyr647Phe)
c.1718A>T (p.Tyr573Phe)
c.1658A>T (p.Tyr553Phe)
c.1829A>T (p.Tyr610Phe)
20g.61928359C>ACA409509286CDH4c.1941C>A (p.Tyr647Ter)
c.1719C>A (p.Tyr573Ter)
c.1659C>A (p.Tyr553Ter)
c.1830C>A (p.Tyr610Ter)
 gnomAD v4
20g.61928359C=CA2373989283CDH4c.1941C= (p.Tyr647=)
c.1719C= (p.Tyr573=)
c.1659C= (p.Tyr553=)
c.1830C= (p.Tyr610=)
20g.61928359C>GCA409509287CDH4c.1941C>G (p.Tyr647Ter)
c.1719C>G (p.Tyr573Ter)
c.1659C>G (p.Tyr553Ter)
c.1830C>G (p.Tyr610Ter)
20g.61928359C>TCA9934914CDH4c.1941C>T (p.Tyr647=)
c.1719C>T (p.Tyr573=)
c.1659C>T (p.Tyr553=)
c.1830C>T (p.Tyr610=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928360G>ACA9934915CDH4c.1942G>A (p.Val648Ile)
c.1720G>A (p.Val574Ile)
c.1660G>A (p.Val554Ile)
c.1831G>A (p.Val611Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928360G>CCA409509288CDH4c.1942G>C (p.Val648Leu)
c.1720G>C (p.Val574Leu)
c.1660G>C (p.Val554Leu)
c.1831G>C (p.Val611Leu)
20g.61928360G=CA2373989284CDH4c.1942G= (p.Val648=)
c.1720G= (p.Val574=)
c.1660G= (p.Val554=)
c.1831G= (p.Val611=)
20g.61928360G>TCA409509289CDH4c.1942G>T (p.Val648Phe)
c.1720G>T (p.Val574Phe)
c.1660G>T (p.Val554Phe)
c.1831G>T (p.Val611Phe)
 gnomAD v4

Number of alleles fetched