Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.54277981C>G | CA16602385 | PDGFRA | c.1977C>G (p.Asn659Lys) n.215C>G c.1257C>G (p.Asn419Lys) n.403C>G n.1795C>G c.2052C>G (p.Asn684Lys) c.2016C>G (p.Asn672Lys) | ClinVar dbSNP COSMIC |
4 | g.54277981C>A | CA16602384 | PDGFRA | c.1977C>A (p.Asn659Lys) n.215C>A c.1257C>A (p.Asn419Lys) n.403C>A n.1795C>A c.2052C>A (p.Asn684Lys) c.2016C>A (p.Asn672Lys) | ClinVar dbSNP COSMIC |