Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674242A>T | CA397839091 | TP53 | c.721T>A (p.Ser241Thr) c.325T>A (p.Ser109Thr) c.442T>A (p.Ser148Thr) c.700T>A (p.Ser234Thr) c.604T>A (p.Ser202Thr) c.244T>A (p.Ser82Thr) c.688T>A (p.Ser230Thr) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674242A>C | CA16603080 | TP53 | c.721T>G (p.Ser241Ala) c.325T>G (p.Ser109Ala) c.442T>G (p.Ser148Ala) c.700T>G (p.Ser234Ala) c.604T>G (p.Ser202Ala) c.244T>G (p.Ser82Ala) c.688T>G (p.Ser230Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674242A>G | CA16603079 | TP53 | c.721T>C (p.Ser241Pro) c.325T>C (p.Ser109Pro) c.442T>C (p.Ser148Pro) c.700T>C (p.Ser234Pro) c.604T>C (p.Ser202Pro) c.244T>C (p.Ser82Pro) c.688T>C (p.Ser230Pro) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |