Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.61928394G>C | CA16609544 | CDH4 | c.1976G>C (p.Arg659Pro) c.1754G>C (p.Arg585Pro) c.1694G>C (p.Arg565Pro) c.1865G>C (p.Arg622Pro) | ClinVar dbSNP gnomAD v4 |
20 | g.61928394G>A | CA9934930 | CDH4 | c.1976G>A (p.Arg659Gln) c.1754G>A (p.Arg585Gln) c.1694G>A (p.Arg565Gln) c.1865G>A (p.Arg622Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |