Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81752250C>T | CA257399 | HGF | c.495G>A (p.Ser165=) c.483-3G>A (n.483-3G>A) n.511-3G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.81752250C>A | CA456129497 | HGF | c.495G>T (p.Ser165=) c.483-3G>T (n.483-3G>T) n.511-3G>T | dbSNP |
7 | g.81752250C>G | CA456129498 | HGF | c.495G>C (p.Ser165=) c.483-3G>C (n.483-3G>C) n.511-3G>C | dbSNP |