| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674918A>C | CA16603100 | TP53 | c.613T>G (p.Tyr205Asp) c.217T>G (p.Tyr73Asp) c.334T>G (p.Tyr112Asp) c.592T>G (p.Tyr198Asp) n.869T>G n.67+135T>G c.496T>G (p.Tyr166Asp) c.136T>G (p.Tyr46Asp) c.580T>G (p.Tyr194Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674918A>T | CA16603098 | TP53 | c.613T>A (p.Tyr205Asn) c.217T>A (p.Tyr73Asn) c.334T>A (p.Tyr112Asn) c.592T>A (p.Tyr198Asn) n.869T>A n.67+135T>A c.496T>A (p.Tyr166Asn) c.136T>A (p.Tyr46Asn) c.580T>A (p.Tyr194Asn) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674918A>G | CA16603099 | TP53 | c.613T>C (p.Tyr205His) c.217T>C (p.Tyr73His) c.334T>C (p.Tyr112His) c.592T>C (p.Tyr198His) n.869T>C n.67+135T>C c.496T>C (p.Tyr166His) c.136T>C (p.Tyr46His) c.580T>C (p.Tyr194His) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |