| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673784C>A | CA397836868 | TP53 | c.836G>T (p.Gly279Val) c.440G>T (p.Gly147Val) c.557G>T (p.Gly186Val) c.815G>T (p.Gly272Val) c.782+397G>T (n.782+397G>T) c.719G>T (p.Gly240Val) c.359G>T (p.Gly120Val) c.803G>T (p.Gly268Val) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673784C>T | CA16620616 | TP53 | c.836G>A (p.Gly279Glu) c.440G>A (p.Gly147Glu) c.557G>A (p.Gly186Glu) c.815G>A (p.Gly272Glu) c.782+397G>A (n.782+397G>A) c.719G>A (p.Gly240Glu) c.359G>A (p.Gly120Glu) c.803G>A (p.Gly268Glu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |