Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.177095415C>G | CA16602607 | FGFR4 | c.1605C>G (p.Asn535Lys) c.1485C>G (p.Asn495Lys) c.1401C>G (p.Asn467Lys) n.591C>G c.499C>G c.1698C>G (p.Asn566Lys) c.1287C>G (p.Asn429Lys) n.1600C>G | ClinVar dbSNP COSMIC COSMIC |
5 | g.177095415C>T | CA447725470 | FGFR4 | c.1605C>T (p.Asn535=) c.1485C>T (p.Asn495=) c.1401C>T (p.Asn467=) n.591C>T c.499C>T c.1698C>T (p.Asn566=) c.1287C>T (p.Asn429=) n.1600C>T | dbSNP gnomAD v3 gnomAD v4 |
5 | g.177095415C>A | CA16602606 | FGFR4 | c.1605C>A (p.Asn535Lys) c.1485C>A (p.Asn495Lys) c.1401C>A (p.Asn467Lys) n.591C>A c.499C>A c.1698C>A (p.Asn566Lys) c.1287C>A (p.Asn429Lys) n.1600C>A | ClinVar dbSNP COSMIC COSMIC |