Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674946G>T | CA497925357 | TP53 | c.585C>A (p.Ile195=) c.189C>A (p.Ile63=) c.306C>A (p.Ile102=) c.564C>A (p.Ile188=) n.841C>A n.67+107C>A c.468C>A (p.Ile156=) c.108C>A (p.Ile36=) c.552C>A (p.Ile184=) | ClinVar dbSNP |
17 | g.7674946G>C | CA16603040 | TP53 | c.585C>G (p.Ile195Met) c.189C>G (p.Ile63Met) c.306C>G (p.Ile102Met) c.564C>G (p.Ile188Met) n.841C>G n.67+107C>G c.468C>G (p.Ile156Met) c.108C>G (p.Ile36Met) c.552C>G (p.Ile184Met) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674946G>A | CA497925355 | TP53 | c.585C>T (p.Ile195=) c.189C>T (p.Ile63=) c.306C>T (p.Ile102=) c.564C>T (p.Ile188=) n.841C>T n.67+107C>T c.468C>T (p.Ile156=) c.108C>T (p.Ile36=) c.552C>T (p.Ile184=) | dbSNP |