| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673812A>C | CA16603020 | TP53 | c.808T>G (p.Phe270Val) c.412T>G (p.Phe138Val) c.529T>G (p.Phe177Val) c.787T>G (p.Phe263Val) c.782+369T>G (n.782+369T>G) c.691T>G (p.Phe231Val) c.331T>G (p.Phe111Val) c.775T>G (p.Phe259Val) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673812A>G | CA397837052 | TP53 | c.808T>C (p.Phe270Leu) c.412T>C (p.Phe138Leu) c.529T>C (p.Phe177Leu) c.787T>C (p.Phe263Leu) c.782+369T>C (n.782+369T>C) c.691T>C (p.Phe231Leu) c.331T>C (p.Phe111Leu) c.775T>C (p.Phe259Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673812A>T | CA16603018 | TP53 | c.808T>A (p.Phe270Ile) c.412T>A (p.Phe138Ile) c.529T>A (p.Phe177Ile) c.787T>A (p.Phe263Ile) c.782+369T>A (n.782+369T>A) c.691T>A (p.Phe231Ile) c.331T>A (p.Phe111Ile) c.775T>A (p.Phe259Ile) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |