Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68829701A>TCA151521CDH1c.2343A>T (p.Glu781Asp)
c.2160A>T (p.Glu720Asp)
n.561A>T
n.2414A>T
c.*1009A>T (p.=)
c.*583A>T (p.=)
c.2406A>T (p.Glu802Asp)
c.1853+3147A>T (p.=)
c.1866-4502A>T (p.=)
c.1608A>T (p.Glu536Asp)
c.795A>T (p.Glu265Asp)
c.378A>T (p.Glu126Asp)
ClinVar dbSNP ExAC gnomAD
16g.68829701A>GCA189425CDH1c.2343A>G (p.Glu781=)
c.2160A>G (p.Glu720=)
n.561A>G
n.2414A>G
c.*1009A>G (p.=)
c.*583A>G (p.=)
c.2406A>G (p.Glu802=)
c.1853+3147A>G (p.=)
c.1866-4502A>G (p.=)
c.1608A>G (p.Glu536=)
c.795A>G (p.Glu265=)
c.378A>G (p.Glu126=)
ClinVar dbSNP

Number of alleles fetched