| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674226A>T | CA397839001 | TP53 | c.737T>A (p.Met246Lys) c.341T>A (p.Met114Lys) c.458T>A (p.Met153Lys) c.716T>A (p.Met239Lys) c.620T>A (p.Met207Lys) c.260T>A (p.Met87Lys) c.704T>A (p.Met235Lys) | ClinVar dbSNP COSMIC |
| 17 | g.7674226A>C | CA000376 | TP53 | c.737T>G (p.Met246Arg) c.341T>G (p.Met114Arg) c.458T>G (p.Met153Arg) c.716T>G (p.Met239Arg) c.620T>G (p.Met207Arg) c.260T>G (p.Met87Arg) c.704T>G (p.Met235Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674226A>G | CA397838998 | TP53 | c.737T>C (p.Met246Thr) c.341T>C (p.Met114Thr) c.458T>C (p.Met153Thr) c.716T>C (p.Met239Thr) c.620T>C (p.Met207Thr) c.260T>C (p.Met87Thr) c.704T>C (p.Met235Thr) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |