| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674218T>A | CA000389 | TP53 | c.745A>T (p.Arg249Trp) c.349A>T (p.Arg117Trp) c.466A>T (p.Arg156Trp) c.724A>T (p.Arg242Trp) c.466A>T c.628A>T (p.Arg210Trp) c.268A>T (p.Arg90Trp) c.712A>T (p.Arg238Trp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674218T>C | CA16603071 | TP53 | c.745A>G (p.Arg249Gly) c.349A>G (p.Arg117Gly) c.466A>G (p.Arg156Gly) c.724A>G (p.Arg242Gly) c.466A>G c.628A>G (p.Arg210Gly) c.268A>G (p.Arg90Gly) c.712A>G (p.Arg238Gly) | ClinVar dbSNP gnomAD v4 |
| 17 | g.7674218T= | CA2245951351 | TP53 | c.745A= (p.Arg249=) c.349A= (p.Arg117=) c.466A= (p.Arg156=) c.724A= (p.Arg242=) c.466A= c.628A= (p.Arg210=) c.268A= (p.Arg90=) c.712A= (p.Arg238=) | dbSNP |
| 17 | g.7674218T>G | CA497717275 | TP53 | c.745A>C (p.Arg249=) c.349A>C (p.Arg117=) c.466A>C (p.Arg156=) c.724A>C (p.Arg242=) c.466A>C c.628A>C (p.Arg210=) c.268A>C (p.Arg90=) c.712A>C (p.Arg238=) | ClinVar dbSNP COSMIC |