| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673781C>T | CA16603072 | TP53 | c.839G>A (p.Arg280Lys) c.443G>A (p.Arg148Lys) c.560G>A (p.Arg187Lys) c.818G>A (p.Arg273Lys) c.782+400G>A (n.782+400G>A) c.722G>A (p.Arg241Lys) c.362G>A (p.Arg121Lys) c.806G>A (p.Arg269Lys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673781C>G | CA000445 | TP53 | c.839G>C (p.Arg280Thr) c.443G>C (p.Arg148Thr) c.560G>C (p.Arg187Thr) c.818G>C (p.Arg273Thr) c.782+400G>C (n.782+400G>C) c.722G>C (p.Arg241Thr) c.362G>C (p.Arg121Thr) c.806G>C (p.Arg269Thr) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673781C>A | CA000447 | TP53 | c.839G>T (p.Arg280Ile) c.443G>T (p.Arg148Ile) c.560G>T (p.Arg187Ile) c.818G>T (p.Arg273Ile) c.782+400G>T (n.782+400G>T) c.722G>T (p.Arg241Ile) c.362G>T (p.Arg121Ile) c.806G>T (p.Arg269Ile) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |