Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68810290G>TCA121997CDH1c.781G>T (p.Glu261Ter)
n.455-1394G>T
n.852G>T
c.625G>T (p.Glu209Ter)
c.46G>T (p.Glu16Ter)
c.-835G>T (p.=)
c.-1039G>T (p.=)
ClinVar dbSNP COSMIC
16g.68810290G>ACA8129931CDH1c.781G>A (p.Glu261Lys)
n.455-1394G>A
n.852G>A
c.625G>A (p.Glu209Lys)
c.46G>A (p.Glu16Lys)
c.-835G>A (p.=)
c.-1039G>A (p.=)
ClinVar dbSNP ExAC gnomAD COSMIC

Number of alleles fetched