| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674208A>T | CA397838870 | TP53 | c.755T>A (p.Leu252His) c.359T>A (p.Leu120His) c.476T>A (p.Leu159His) c.734T>A (p.Leu245His) c.638T>A (p.Leu213His) c.278T>A (p.Leu93His) c.722T>A (p.Leu241His) | dbSNP COSMIC |
| 17 | g.7674208A>G | CA000398 | TP53 | c.755T>C (p.Leu252Pro) c.359T>C (p.Leu120Pro) c.476T>C (p.Leu159Pro) c.734T>C (p.Leu245Pro) c.638T>C (p.Leu213Pro) c.278T>C (p.Leu93Pro) c.722T>C (p.Leu241Pro) | ClinVar dbSNP COSMIC COSMIC |
| 17 | g.7674208A= | CA2245951226 | TP53 | c.755T= (p.Leu252=) c.359T= (p.Leu120=) c.476T= (p.Leu159=) c.734T= (p.Leu245=) c.638T= (p.Leu213=) c.278T= (p.Leu93=) c.722T= (p.Leu241=) | dbSNP |