Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.68681065A>G | CA8129200 | CDH3 | c.965A>G (p.Asn322Ser) c.*703A>G (n.*703A>G) c.441A>G c.800A>G (p.Asn267Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.68681065A>T | CA127317 | CDH3 | c.965A>T (p.Asn322Ile) c.*703A>T (n.*703A>T) c.441A>T c.800A>T (p.Asn267Ile) | ClinVar dbSNP |