| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177097533G>A | CA3576772 | FGFR4 | c.2266G>A (p.Asp756Asn) c.2146G>A (p.Asp716Asn) c.2062G>A (p.Asp688Asn) n.214G>A c.2359G>A (p.Asp787Asn) c.1948G>A (p.Asp650Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 5 | g.177097533G= | CA1603407682 | FGFR4 | c.2266G= (p.Asp756=) c.2146G= (p.Asp716=) c.2062G= (p.Asp688=) n.214G= c.2359G= (p.Asp787=) c.1948G= (p.Asp650=) | dbSNP |