Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68737363_68737367dupCA16620223CDH1c.-53_-49dup (p.=)
c.-1668_-1664dup (p.=)
c.-1872_-1868dup (p.=)
ClinVar dbSNP
16g.68737363G=CA2229914945CDH1c.-53G= (p.=)
c.-1668G= (p.=)
c.-1872G= (p.=)
16g.68737371_68737375dupCA298936CDH1c.-45_-41dup (p.=)
c.-1660_-1656dup (p.=)
c.-1864_-1860dup (p.=)
ClinVar dbSNP dbSNP gnomAD
16g.68737365C=CA2229914951CDH1c.-51C= (p.=)
c.-1666C= (p.=)
c.-1870C= (p.=)
16g.68737365C>GCA623139877CDH1c.-51C>G (p.=)
c.-1666C>G (p.=)
c.-1870C>G (p.=)
gnomAD
16g.68737365C>TCA623139875CDH1c.-51C>T (p.=)
c.-1666C>T (p.=)
c.-1870C>T (p.=)
gnomAD
16g.68737366C>ACA723156551CDH1c.-50C>A (p.=)
c.-1665C>A (p.=)
c.-1869C>A (p.=)
16g.68737366C=CA2229914957CDH1c.-50C= (p.=)
c.-1665C= (p.=)
c.-1869C= (p.=)
16g.68737366C>GCA10577530CDH1c.-50C>G (p.=)
c.-1665C>G (p.=)
c.-1869C>G (p.=)
ClinVar dbSNP
16g.68737366C>TCA16620222CDH1c.-50C>T (p.=)
c.-1665C>T (p.=)
c.-1869C>T (p.=)
ClinVar dbSNP gnomAD
16g.68737367G>ACA723156560CDH1c.-49G>A (p.=)
c.-1664G>A (p.=)
c.-1868G>A (p.=)
16g.68737367G=CA2229914964CDH1c.-49G= (p.=)
c.-1664G= (p.=)
c.-1868G= (p.=)
16g.68737367G>TCA10583398CDH1c.-49G>T (p.=)
c.-1664G>T (p.=)
c.-1868G>T (p.=)
ClinVar dbSNP gnomAD
16g.68737368A=CA2229914968CDH1c.-48A= (p.=)
c.-1663A= (p.=)
c.-1867A= (p.=)
16g.68737368A>GCA2229914969CDH1c.-48A>G (p.=)
c.-1663A>G (p.=)
c.-1867A>G (p.=)
16g.68737369C=CA2229914974CDH1c.-47C= (p.=)
c.-1662C= (p.=)
c.-1866C= (p.=)
16g.68737369C>TCA16620224CDH1c.-47C>T (p.=)
c.-1662C>T (p.=)
c.-1866C>T (p.=)
ClinVar
16g.68737370C=CA2229914976CDH1c.-46C= (p.=)
c.-1661C= (p.=)
c.-1865C= (p.=)
16g.68737370C>TCA283273290CDH1c.-46C>T (p.=)
c.-1661C>T (p.=)
c.-1865C>T (p.=)
dbSNP
16g.68737371C=CA2229914978CDH1c.-45C= (p.=)
c.-1660C= (p.=)
c.-1864C= (p.=)
16g.68737371C>TCA16620225CDH1c.-45C>T (p.=)
c.-1660C>T (p.=)
c.-1864C>T (p.=)
ClinVar
16g.68737372G>ACA10603546CDH1c.-44G>A (p.=)
c.-1659G>A (p.=)
c.-1863G>A (p.=)
ClinVar dbSNP gnomAD
16g.68737372G>CCA623139882CDH1c.-44G>C (p.=)
c.-1659G>C (p.=)
c.-1863G>C (p.=)
gnomAD
16g.68737372G=CA2229914981CDH1c.-44G= (p.=)
c.-1659G= (p.=)
c.-1863G= (p.=)
16g.68737373A=CA2229914988CDH1c.-43A= (p.=)
c.-1658A= (p.=)
c.-1862A= (p.=)
16g.68737373A>GCA978517789CDH1c.-43A>G (p.=)
c.-1658A>G (p.=)
c.-1862A>G (p.=)
16g.68737374C=CA2229914989CDH1c.-42C= (p.=)
c.-1657C= (p.=)
c.-1861C= (p.=)
16g.68737374C>TCA496149545CDH1c.-42C>T (p.=)
c.-1657C>T (p.=)
c.-1861C>T (p.=)
16g.68737375C>ACA298960CDH1c.-41C>A (p.=)
c.-1656C>A (p.=)
c.-1860C>A (p.=)
ClinVar dbSNP gnomAD
16g.68737375C=CA2229914990CDH1c.-41C= (p.=)
c.-1656C= (p.=)
c.-1860C= (p.=)
16g.68737375C>GCA2229914991CDH1c.-41C>G (p.=)
c.-1656C>G (p.=)
c.-1860C>G (p.=)
16g.68737376G>ACA16607041CDH1c.-40G>A (p.=)
c.-1655G>A (p.=)
c.-1859G>A (p.=)
ClinVar gnomAD
16g.68737376G=CA2229914993CDH1c.-40G= (p.=)
c.-1655G= (p.=)
c.-1859G= (p.=)
16g.68737377C=CA2229914995CDH1c.-39C= (p.=)
c.-1654C= (p.=)
c.-1858C= (p.=)
16g.68737377C>TCA8129769CDH1c.-39C>T (p.=)
c.-1654C>T (p.=)
c.-1858C>T (p.=)
ClinVar dbSNP ExAC gnomAD
16g.68737378A=CA2229914998CDH1c.-38A= (p.=)
c.-1653A= (p.=)
c.-1857A= (p.=)
16g.68737379C>ACA16607325CDH1c.-37C>A (p.=)
c.-1652C>A (p.=)
c.-1856C>A (p.=)
ClinVar
16g.68737379C=CA2229915001CDH1c.-37C= (p.=)
c.-1652C= (p.=)
c.-1856C= (p.=)
16g.68737379C>TCA623139886CDH1c.-37C>T (p.=)
c.-1652C>T (p.=)
c.-1856C>T (p.=)
gnomAD
16g.68737381dupCA8129770CDH1c.-35dup (p.=)
c.-1650dup (p.=)
c.-1854dup (p.=)
dbSNP ExAC gnomAD
16g.68737380C=CA2229915005CDH1c.-36C= (p.=)
c.-1651C= (p.=)
c.-1855C= (p.=)
16g.68737380C>TCA10577532CDH1c.-36C>T (p.=)
c.-1651C>T (p.=)
c.-1855C>T (p.=)
ClinVar dbSNP
16g.68737381C=CA2229915008CDH1c.-35C= (p.=)
c.-1650C= (p.=)
c.-1854C= (p.=)
16g.68737381C>TCA283273331CDH1c.-35C>T (p.=)
c.-1650C>T (p.=)
c.-1854C>T (p.=)
dbSNP gnomAD
16g.68737382G>ACA623139887CDH1c.-34G>A (p.=)
c.-1649G>A (p.=)
c.-1853G>A (p.=)
gnomAD
16g.68737382G=CA2229915010CDH1c.-34G= (p.=)
c.-1649G= (p.=)
c.-1853G= (p.=)
16g.68737383G=CA2229915013CDH1c.-33G= (p.=)
c.-1648G= (p.=)
c.-1852G= (p.=)
16g.68737383G>TCA623139889CDH1c.-33G>T (p.=)
c.-1648G>T (p.=)
c.-1852G>T (p.=)
ClinVar gnomAD
16g.68737384C=CA2229915018CDH1c.-32C= (p.=)
c.-1647C= (p.=)
c.-1851C= (p.=)
16g.68737384C>GCA16608216CDH1c.-32C>G (p.=)
c.-1647C>G (p.=)
c.-1851C>G (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched