| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674216C>G | CA16615944 | TP53 | c.747G>C (p.Arg249Ser) c.351G>C (p.Arg117Ser) c.468G>C (p.Arg156Ser) c.726G>C (p.Arg242Ser) c.630G>C (p.Arg210Ser) c.270G>C (p.Arg90Ser) c.714G>C (p.Arg238Ser) | ClinVar dbSNP |
| 17 | g.7674216C>T | CA497717264 | TP53 | c.747G>A (p.Arg249=) c.351G>A (p.Arg117=) c.468G>A (p.Arg156=) c.726G>A (p.Arg242=) c.630G>A (p.Arg210=) c.270G>A (p.Arg90=) c.714G>A (p.Arg238=) | ClinVar dbSNP COSMIC |
| 17 | g.7674216C>A | CA000392 | TP53 | c.747G>T (p.Arg249Ser) c.351G>T (p.Arg117Ser) c.468G>T (p.Arg156Ser) c.726G>T (p.Arg242Ser) c.630G>T (p.Arg210Ser) c.270G>T (p.Arg90Ser) c.714G>T (p.Arg238Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |