Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68819293A>CCA496154305CDH1c.1579A>C (p.Arg527=)
c.1396A>C (p.Arg466=)
n.1650A>C
c.*245A>C (p.=)
c.1566-2708A>C (p.=)
c.1642A>C (p.Arg548=)
c.844A>C (p.Arg282=)
c.31A>C (p.Arg11=)
c.-254-2708A>C (p.=)
16g.68819293A>GCA396464862CDH1c.1579A>G (p.Arg527Gly)
c.1396A>G (p.Arg466Gly)
n.1650A>G
c.*245A>G (p.=)
c.1566-2708A>G (p.=)
c.1642A>G (p.Arg548Gly)
c.844A>G (p.Arg282Gly)
c.31A>G (p.Arg11Gly)
c.-254-2708A>G (p.=)
16g.68819293A>TCA396464859CDH1c.1579A>T (p.Arg527Ter)
c.1396A>T (p.Arg466Ter)
n.1650A>T
c.*245A>T (p.=)
c.1566-2708A>T (p.=)
c.1642A>T (p.Arg548Ter)
c.844A>T (p.Arg282Ter)
c.31A>T (p.Arg11Ter)
c.-254-2708A>T (p.=)
16g.68819294G>ACA396464868CDH1c.1580G>A (p.Arg527Lys)
c.1397G>A (p.Arg466Lys)
n.1651G>A
c.*246G>A (p.=)
c.1566-2707G>A (p.=)
c.1643G>A (p.Arg548Lys)
c.845G>A (p.Arg282Lys)
c.32G>A (p.Arg11Lys)
c.-254-2707G>A (p.=)
16g.68819294G>CCA396464864CDH1c.1580G>C (p.Arg527Thr)
c.1397G>C (p.Arg466Thr)
n.1651G>C
c.*246G>C (p.=)
c.1566-2707G>C (p.=)
c.1643G>C (p.Arg548Thr)
c.845G>C (p.Arg282Thr)
c.32G>C (p.Arg11Thr)
c.-254-2707G>C (p.=)
16g.68819294G>TCA396464871CDH1c.1580G>T (p.Arg527Ile)
c.1397G>T (p.Arg466Ile)
n.1651G>T
c.*246G>T (p.=)
c.1566-2707G>T (p.=)
c.1643G>T (p.Arg548Ile)
c.845G>T (p.Arg282Ile)
c.32G>T (p.Arg11Ile)
c.-254-2707G>T (p.=)
16g.68819295A>CCA396464872CDH1c.1581A>C (p.Arg527Ser)
c.1398A>C (p.Arg466Ser)
n.1652A>C
c.*247A>C (p.=)
c.1566-2706A>C (p.=)
c.1644A>C (p.Arg548Ser)
c.846A>C (p.Arg282Ser)
c.33A>C (p.Arg11Ser)
c.-254-2706A>C (p.=)
16g.68819295A>GCA496154307CDH1c.1581A>G (p.Arg527=)
c.1398A>G (p.Arg466=)
n.1652A>G
c.*247A>G (p.=)
c.1566-2706A>G (p.=)
c.1644A>G (p.Arg548=)
c.846A>G (p.Arg282=)
c.33A>G (p.Arg11=)
c.-254-2706A>G (p.=)
ClinVar
16g.68819295A>TCA396464873CDH1c.1581A>T (p.Arg527Ser)
c.1398A>T (p.Arg466Ser)
n.1652A>T
c.*247A>T (p.=)
c.1566-2706A>T (p.=)
c.1644A>T (p.Arg548Ser)
c.846A>T (p.Arg282Ser)
c.33A>T (p.Arg11Ser)
c.-254-2706A>T (p.=)
16g.68819296G>ACA396464874CDH1c.1582G>A (p.Asp528Asn)
c.1399G>A (p.Asp467Asn)
n.1653G>A
c.*248G>A (p.=)
c.1566-2705G>A (p.=)
c.1645G>A (p.Asp549Asn)
c.847G>A (p.Asp283Asn)
c.34G>A (p.Asp12Asn)
c.-254-2705G>A (p.=)
16g.68819296G>CCA396464875CDH1c.1582G>C (p.Asp528His)
c.1399G>C (p.Asp467His)
n.1653G>C
c.*248G>C (p.=)
c.1566-2705G>C (p.=)
c.1645G>C (p.Asp549His)
c.847G>C (p.Asp283His)
c.34G>C (p.Asp12His)
c.-254-2705G>C (p.=)
16g.68819296G=CA2229977845CDH1c.1582G= (p.Asp528=)
c.1399G= (p.Asp467=)
n.1653G=
c.*248G= (p.=)
c.1566-2705G= (p.=)
c.1645G= (p.Asp549=)
c.847G= (p.Asp283=)
c.34G= (p.Asp12=)
c.-254-2705G= (p.=)
16g.68819296G>TCA396464876CDH1c.1582G>T (p.Asp528Tyr)
c.1399G>T (p.Asp467Tyr)
n.1653G>T
c.*248G>T (p.=)
c.1566-2705G>T (p.=)
c.1645G>T (p.Asp549Tyr)
c.847G>T (p.Asp283Tyr)
c.34G>T (p.Asp12Tyr)
c.-254-2705G>T (p.=)
16g.68819297A>CCA396464877CDH1c.1583A>C (p.Asp528Ala)
c.1400A>C (p.Asp467Ala)
n.1654A>C
c.*249A>C (p.=)
c.1566-2704A>C (p.=)
c.1646A>C (p.Asp549Ala)
c.848A>C (p.Asp283Ala)
c.35A>C (p.Asp12Ala)
c.-254-2704A>C (p.=)
16g.68819297A>GCA396464878CDH1c.1583A>G (p.Asp528Gly)
c.1400A>G (p.Asp467Gly)
n.1654A>G
c.*249A>G (p.=)
c.1566-2704A>G (p.=)
c.1646A>G (p.Asp549Gly)
c.848A>G (p.Asp283Gly)
c.35A>G (p.Asp12Gly)
c.-254-2704A>G (p.=)
16g.68819297A>TCA396464880CDH1c.1583A>T (p.Asp528Val)
c.1400A>T (p.Asp467Val)
n.1654A>T
c.*249A>T (p.=)
c.1566-2704A>T (p.=)
c.1646A>T (p.Asp549Val)
c.848A>T (p.Asp283Val)
c.35A>T (p.Asp12Val)
c.-254-2704A>T (p.=)
16g.68819298C>ACA396464881CDH1c.1584C>A (p.Asp528Glu)
c.1401C>A (p.Asp467Glu)
n.1655C>A
c.*250C>A (p.=)
c.1566-2703C>A (p.=)
c.1647C>A (p.Asp549Glu)
c.849C>A (p.Asp283Glu)
c.36C>A (p.Asp12Glu)
c.-254-2703C>A (p.=)
16g.68819298C=CA2229977849CDH1c.1584C= (p.Asp528=)
c.1401C= (p.Asp467=)
n.1655C=
c.*250C= (p.=)
c.1566-2703C= (p.=)
c.1647C= (p.Asp549=)
c.849C= (p.Asp283=)
c.36C= (p.Asp12=)
c.-254-2703C= (p.=)
16g.68819298C>GCA396464884CDH1c.1584C>G (p.Asp528Glu)
c.1401C>G (p.Asp467Glu)
n.1655C>G
c.*250C>G (p.=)
c.1566-2703C>G (p.=)
c.1647C>G (p.Asp549Glu)
c.849C>G (p.Asp283Glu)
c.36C>G (p.Asp12Glu)
c.-254-2703C>G (p.=)
16g.68819298C>TCA496154308CDH1c.1584C>T (p.Asp528=)
c.1401C>T (p.Asp467=)
n.1655C>T
c.*250C>T (p.=)
c.1566-2703C>T (p.=)
c.1647C>T (p.Asp549=)
c.849C>T (p.Asp283=)
c.36C>T (p.Asp12=)
c.-254-2703C>T (p.=)
gnomAD
16g.68819299A=CA2229977855CDH1c.1585A= (p.Thr529=)
c.1402A= (p.Thr468=)
n.1656A=
c.*251A= (p.=)
c.1566-2702A= (p.=)
c.1648A= (p.Thr550=)
c.850A= (p.Thr284=)
c.37A= (p.Thr13=)
c.-254-2702A= (p.=)
16g.68819299A>CCA194038CDH1c.1585A>C (p.Thr529Pro)
c.1402A>C (p.Thr468Pro)
n.1656A>C
c.*251A>C (p.=)
c.1566-2702A>C (p.=)
c.1648A>C (p.Thr550Pro)
c.850A>C (p.Thr284Pro)
c.37A>C (p.Thr13Pro)
c.-254-2702A>C (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68819299A>GCA347984CDH1c.1585A>G (p.Thr529Ala)
c.1402A>G (p.Thr468Ala)
n.1656A>G
c.*251A>G (p.=)
c.1566-2702A>G (p.=)
c.1648A>G (p.Thr550Ala)
c.850A>G (p.Thr284Ala)
c.37A>G (p.Thr13Ala)
c.-254-2702A>G (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68819299A>TCA396464890CDH1c.1585A>T (p.Thr529Ser)
c.1402A>T (p.Thr468Ser)
n.1656A>T
c.*251A>T (p.=)
c.1566-2702A>T (p.=)
c.1648A>T (p.Thr550Ser)
c.850A>T (p.Thr284Ser)
c.37A>T (p.Thr13Ser)
c.-254-2702A>T (p.=)
16g.68819300C>ACA396464893CDH1c.1586C>A (p.Thr529Asn)
c.1403C>A (p.Thr468Asn)
n.1657C>A
c.*252C>A (p.=)
c.1566-2701C>A (p.=)
c.1649C>A (p.Thr550Asn)
c.851C>A (p.Thr284Asn)
c.38C>A (p.Thr13Asn)
c.-254-2701C>A (p.=)
16g.68819300C=CA2229977863CDH1c.1586C= (p.Thr529=)
c.1403C= (p.Thr468=)
n.1657C=
c.*252C= (p.=)
c.1566-2701C= (p.=)
c.1649C= (p.Thr550=)
c.851C= (p.Thr284=)
c.38C= (p.Thr13=)
c.-254-2701C= (p.=)
16g.68819300C>GCA396464895CDH1c.1586C>G (p.Thr529Ser)
c.1403C>G (p.Thr468Ser)
n.1657C>G
c.*252C>G (p.=)
c.1566-2701C>G (p.=)
c.1649C>G (p.Thr550Ser)
c.851C>G (p.Thr284Ser)
c.38C>G (p.Thr13Ser)
c.-254-2701C>G (p.=)
16g.68819300C>TCA396464897CDH1c.1586C>T (p.Thr529Ile)
c.1403C>T (p.Thr468Ile)
n.1657C>T
c.*252C>T (p.=)
c.1566-2701C>T (p.=)
c.1649C>T (p.Thr550Ile)
c.851C>T (p.Thr284Ile)
c.38C>T (p.Thr13Ile)
c.-254-2701C>T (p.=)
ClinVar
16g.68819301T>ACA496154311CDH1c.1587T>A (p.Thr529=)
c.1404T>A (p.Thr468=)
n.1658T>A
c.*253T>A (p.=)
c.1566-2700T>A (p.=)
c.1650T>A (p.Thr550=)
c.852T>A (p.Thr284=)
c.39T>A (p.Thr13=)
c.-254-2700T>A (p.=)
16g.68819301T>CCA283310311CDH1c.1587T>C (p.Thr529=)
c.1404T>C (p.Thr468=)
n.1658T>C
c.*253T>C (p.=)
c.1566-2700T>C (p.=)
c.1650T>C (p.Thr550=)
c.852T>C (p.Thr284=)
c.39T>C (p.Thr13=)
c.-254-2700T>C (p.=)
ClinVar dbSNP gnomAD
16g.68819301T>GCA496154313CDH1c.1587T>G (p.Thr529=)
c.1404T>G (p.Thr468=)
n.1658T>G
c.*253T>G (p.=)
c.1566-2700T>G (p.=)
c.1650T>G (p.Thr550=)
c.852T>G (p.Thr284=)
c.39T>G (p.Thr13=)
c.-254-2700T>G (p.=)
16g.68819301T=CA2229977872CDH1c.1587T= (p.Thr529=)
c.1404T= (p.Thr468=)
n.1658T=
c.*253T= (p.=)
c.1566-2700T= (p.=)
c.1650T= (p.Thr550=)
c.852T= (p.Thr284=)
c.39T= (p.Thr13=)
c.-254-2700T= (p.=)
16g.68819301dupCA16620251CDH1c.1587dup (p.Ala530CysfsTer7)
c.1404dup (p.Ala469CysfsTer7)
n.1658dup
c.*253dup (p.=)
c.1566-2700dup (p.=)
c.1650dup (p.Ala551CysfsTer7)
c.852dup (p.Ala285CysfsTer7)
c.39dup (p.Ala14CysfsTer7)
c.-254-2700dup (p.=)
ClinVar dbSNP
16g.68819302G>ACA396464904CDH1c.1588G>A (p.Ala530Thr)
c.1405G>A (p.Ala469Thr)
n.1659G>A
c.*254G>A (p.=)
c.1566-2699G>A (p.=)
c.1651G>A (p.Ala551Thr)
c.853G>A (p.Ala285Thr)
c.40G>A (p.Ala14Thr)
c.-254-2699G>A (p.=)
16g.68819302G>CCA396464906CDH1c.1588G>C (p.Ala530Pro)
c.1405G>C (p.Ala469Pro)
n.1659G>C
c.*254G>C (p.=)
c.1566-2699G>C (p.=)
c.1651G>C (p.Ala551Pro)
c.853G>C (p.Ala285Pro)
c.40G>C (p.Ala14Pro)
c.-254-2699G>C (p.=)
ClinVar
16g.68819302G=CA2229977877CDH1c.1588G= (p.Ala530=)
c.1405G= (p.Ala469=)
n.1659G=
c.*254G= (p.=)
c.1566-2699G= (p.=)
c.1651G= (p.Ala551=)
c.853G= (p.Ala285=)
c.40G= (p.Ala14=)
c.-254-2699G= (p.=)
16g.68819302G>TCA396464908CDH1c.1588G>T (p.Ala530Ser)
c.1405G>T (p.Ala469Ser)
n.1659G>T
c.*254G>T (p.=)
c.1566-2699G>T (p.=)
c.1651G>T (p.Ala551Ser)
c.853G>T (p.Ala285Ser)
c.40G>T (p.Ala14Ser)
c.-254-2699G>T (p.=)
16g.68819303C>ACA396464910CDH1c.1589C>A (p.Ala530Asp)
c.1406C>A (p.Ala469Asp)
n.1660C>A
c.*255C>A (p.=)
c.1566-2698C>A (p.=)
c.1652C>A (p.Ala551Asp)
c.854C>A (p.Ala285Asp)
c.41C>A (p.Ala14Asp)
c.-254-2698C>A (p.=)
16g.68819303C=CA2229977886CDH1c.1589C= (p.Ala530=)
c.1406C= (p.Ala469=)
n.1660C=
c.*255C= (p.=)
c.1566-2698C= (p.=)
c.1652C= (p.Ala551=)
c.854C= (p.Ala285=)
c.41C= (p.Ala14=)
c.-254-2698C= (p.=)
16g.68819303C>GCA396464913CDH1c.1589C>G (p.Ala530Gly)
c.1406C>G (p.Ala469Gly)
n.1660C>G
c.*255C>G (p.=)
c.1566-2698C>G (p.=)
c.1652C>G (p.Ala551Gly)
c.854C>G (p.Ala285Gly)
c.41C>G (p.Ala14Gly)
c.-254-2698C>G (p.=)
16g.68819303C>TCA396464916CDH1c.1589C>T (p.Ala530Val)
c.1406C>T (p.Ala469Val)
n.1660C>T
c.*255C>T (p.=)
c.1566-2698C>T (p.=)
c.1652C>T (p.Ala551Val)
c.854C>T (p.Ala285Val)
c.41C>T (p.Ala14Val)
c.-254-2698C>T (p.=)
ClinVar
16g.68819304dupCA658658491CDH1c.1590dup (p.Asn531GlnfsTer6)
c.1407dup (p.Asn470GlnfsTer6)
n.1661dup
c.*256dup (p.=)
c.1566-2697dup (p.=)
c.1653dup (p.Asn552GlnfsTer6)
c.855dup (p.Asn286GlnfsTer6)
c.42dup (p.Asn15GlnfsTer6)
c.-254-2697dup (p.=)
ClinVar dbSNP
16g.68819304C>ACA496154314CDH1c.1590C>A (p.Ala530=)
c.1407C>A (p.Ala469=)
n.1661C>A
c.*256C>A (p.=)
c.1566-2697C>A (p.=)
c.1653C>A (p.Ala551=)
c.855C>A (p.Ala285=)
c.42C>A (p.Ala14=)
c.-254-2697C>A (p.=)
16g.68819304C=CA2229977893CDH1c.1590C= (p.Ala530=)
c.1407C= (p.Ala469=)
n.1661C=
c.*256C= (p.=)
c.1566-2697C= (p.=)
c.1653C= (p.Ala551=)
c.855C= (p.Ala285=)
c.42C= (p.Ala14=)
c.-254-2697C= (p.=)
16g.68819304C>GCA496154315CDH1c.1590C>G (p.Ala530=)
c.1407C>G (p.Ala469=)
n.1661C>G
c.*256C>G (p.=)
c.1566-2697C>G (p.=)
c.1653C>G (p.Ala551=)
c.855C>G (p.Ala285=)
c.42C>G (p.Ala14=)
c.-254-2697C>G (p.=)
16g.68819304C>TCA190534CDH1c.1590C>T (p.Ala530=)
c.1407C>T (p.Ala469=)
n.1661C>T
c.*256C>T (p.=)
c.1566-2697C>T (p.=)
c.1653C>T (p.Ala551=)
c.855C>T (p.Ala285=)
c.42C>T (p.Ala14=)
c.-254-2697C>T (p.=)
ClinVar dbSNP
16g.68819305A>CCA396464922CDH1c.1591A>C (p.Asn531His)
c.1408A>C (p.Asn470His)
n.1662A>C
c.*257A>C (p.=)
c.1566-2696A>C (p.=)
c.1654A>C (p.Asn552His)
c.856A>C (p.Asn286His)
c.43A>C (p.Asn15His)
c.-254-2696A>C (p.=)
16g.68819305A>GCA396464925CDH1c.1591A>G (p.Asn531Asp)
c.1408A>G (p.Asn470Asp)
n.1662A>G
c.*257A>G (p.=)
c.1566-2696A>G (p.=)
c.1654A>G (p.Asn552Asp)
c.856A>G (p.Asn286Asp)
c.43A>G (p.Asn15Asp)
c.-254-2696A>G (p.=)
16g.68819305A>TCA396464927CDH1c.1591A>T (p.Asn531Tyr)
c.1408A>T (p.Asn470Tyr)
n.1662A>T
c.*257A>T (p.=)
c.1566-2696A>T (p.=)
c.1654A>T (p.Asn552Tyr)
c.856A>T (p.Asn286Tyr)
c.43A>T (p.Asn15Tyr)
c.-254-2696A>T (p.=)
16g.68819306A=CA2229977900CDH1c.1592A= (p.Asn531=)
c.1409A= (p.Asn470=)
n.1663A=
c.*258A= (p.=)
c.1566-2695A= (p.=)
c.1655A= (p.Asn552=)
c.857A= (p.Asn286=)
c.44A= (p.Asn15=)
c.-254-2695A= (p.=)

Number of alleles fetched