Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68811859G>ACA10580100CDH1c.1008G>A (p.Glu336=)
c.273G>A (p.Glu91=)
c.-608G>A (p.=)
c.-812G>A (p.=)
n.630G>A
n.1079G>A
c.852G>A (p.Glu284=)
ClinVar dbSNP COSMIC
16g.68811859G>TCA280990CDH1c.1008G>T (p.Glu336Asp)
c.273G>T (p.Glu91Asp)
c.-608G>T (p.=)
c.-812G>T (p.=)
n.630G>T
n.1079G>T
c.852G>T (p.Glu284Asp)
ClinVar dbSNP

Number of alleles fetched