| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674229C>T | CA000371 | TP53 | c.734G>A (p.Gly245Asp) c.338G>A (p.Gly113Asp) c.455G>A (p.Gly152Asp) c.713G>A (p.Gly238Asp) c.617G>A (p.Gly206Asp) c.257G>A (p.Gly86Asp) c.701G>A (p.Gly234Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674229C>G | CA10588670 | TP53 | c.734G>C (p.Gly245Ala) c.338G>C (p.Gly113Ala) c.455G>C (p.Gly152Ala) c.713G>C (p.Gly238Ala) c.617G>C (p.Gly206Ala) c.257G>C (p.Gly86Ala) c.701G>C (p.Gly234Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674229C>A | CA001743 | TP53 | c.734G>T (p.Gly245Val) c.338G>T (p.Gly113Val) c.455G>T (p.Gly152Val) c.713G>T (p.Gly238Val) c.617G>T (p.Gly206Val) c.257G>T (p.Gly86Val) c.701G>T (p.Gly234Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |