| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673800C>G | CA16603092 | TP53 | c.820G>C (p.Val274Leu) c.424G>C (p.Val142Leu) c.541G>C (p.Val181Leu) c.799G>C (p.Val267Leu) c.782+381G>C (n.782+381G>C) c.703G>C (p.Val235Leu) c.343G>C (p.Val115Leu) c.787G>C (p.Val263Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673800C>T | CA397836967 | TP53 | c.820G>A (p.Val274Ile) c.424G>A (p.Val142Ile) c.541G>A (p.Val181Ile) c.799G>A (p.Val267Ile) c.782+381G>A (n.782+381G>A) c.703G>A (p.Val235Ile) c.343G>A (p.Val115Ile) c.787G>A (p.Val263Ile) | ClinVar dbSNP COSMIC |
| 17 | g.7673800C>A | CA16603088 | TP53 | c.820G>T (p.Val274Phe) c.424G>T (p.Val142Phe) c.541G>T (p.Val181Phe) c.799G>T (p.Val267Phe) c.782+381G>T (n.782+381G>T) c.703G>T (p.Val235Phe) c.343G>T (p.Val115Phe) c.787G>T (p.Val263Phe) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |