Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675094A>T | CA16603083 | TP53 | c.518T>A (p.Val173Glu) c.122T>A (p.Val41Glu) c.239T>A (p.Val80Glu) c.497T>A (p.Val166Glu) n.774T>A n.26T>A c.401T>A (p.Val134Glu) c.41T>A (p.Val14Glu) c.485T>A (p.Val162Glu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675094A>G | CA16602486 | TP53 | c.518T>C (p.Val173Ala) c.122T>C (p.Val41Ala) c.239T>C (p.Val80Ala) c.497T>C (p.Val166Ala) n.774T>C n.26T>C c.401T>C (p.Val134Ala) c.41T>C (p.Val14Ala) c.485T>C (p.Val162Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675094A>C | CA16602485 | TP53 | c.518T>G (p.Val173Gly) c.122T>G (p.Val41Gly) c.239T>G (p.Val80Gly) c.497T>G (p.Val166Gly) n.774T>G n.26T>G c.401T>G (p.Val134Gly) c.41T>G (p.Val14Gly) c.485T>G (p.Val162Gly) | ClinVar dbSNP gnomAD v4 |