Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675076T>C | CA16603027 | TP53 | c.536A>G (p.His179Arg) c.140A>G (p.His47Arg) c.257A>G (p.His86Arg) c.515A>G (p.His172Arg) n.792A>G n.44A>G c.419A>G (p.His140Arg) c.59A>G (p.His20Arg) c.503A>G (p.His168Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675076T>A | CA16603029 | TP53 | c.536A>T (p.His179Leu) c.140A>T (p.His47Leu) c.257A>T (p.His86Leu) c.515A>T (p.His172Leu) n.792A>T n.44A>T c.419A>T (p.His140Leu) c.59A>T (p.His20Leu) c.503A>T (p.His168Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675076T>G | CA16603032 | TP53 | c.536A>C (p.His179Pro) c.140A>C (p.His47Pro) c.257A>C (p.His86Pro) c.515A>C (p.His172Pro) n.792A>C n.44A>C c.419A>C (p.His140Pro) c.59A>C (p.His20Pro) c.503A>C (p.His168Pro) | ClinVar dbSNP |