| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7675996T>C | CA397844193 | TP53 | c.373A>G (p.Thr125Ala) c.-21-760A>G (n.-21-760A>G) c.96+386A>G (n.96+386A>G) n.629A>G c.256A>G (p.Thr86Ala) c.340+29A>G (n.340+29A>G) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675996T>A | CA397844190 | TP53 | c.373A>T (p.Thr125Ser) c.-21-760A>T (n.-21-760A>T) c.96+386A>T (n.96+386A>T) n.629A>T c.256A>T (p.Thr86Ser) c.340+29A>T (n.340+29A>T) | dbSNP |
| 17 | g.7675996T>G | CA16603081 | TP53 | c.373A>C (p.Thr125Pro) c.-21-760A>C (n.-21-760A>C) c.96+386A>C (n.96+386A>C) n.629A>C c.256A>C (p.Thr86Pro) c.340+29A>C (n.340+29A>C) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |