| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7675088C>T | CA000251 | TP53 | c.524G>A (p.Arg175His) c.128G>A (p.Arg43His) c.245G>A (p.Arg82His) c.503G>A (p.Arg168His) n.780G>A n.32G>A c.407G>A (p.Arg136His) c.47G>A (p.Arg16His) c.491G>A (p.Arg164His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675088C>A | CA000252 | TP53 | c.524G>T (p.Arg175Leu) c.128G>T (p.Arg43Leu) c.245G>T (p.Arg82Leu) c.503G>T (p.Arg168Leu) n.780G>T n.32G>T c.407G>T (p.Arg136Leu) c.47G>T (p.Arg16Leu) c.491G>T (p.Arg164Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675088C>G | CA397841469 | TP53 | c.524G>C (p.Arg175Pro) c.128G>C (p.Arg43Pro) c.245G>C (p.Arg82Pro) c.503G>C (p.Arg168Pro) n.780G>C n.32G>C c.407G>C (p.Arg136Pro) c.47G>C (p.Arg16Pro) c.491G>C (p.Arg164Pro) | dbSNP gnomAD v4 COSMIC |