Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675200C>G | CA000166 | TP53 | c.412G>C (p.Ala138Pro) c.16G>C (p.Ala6Pro) c.133G>C (p.Ala45Pro) c.391G>C (p.Ala131Pro) n.668G>C c.295G>C (p.Ala99Pro) c.-66G>C (n.-66G>C) c.379G>C (p.Ala127Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675200C>A | CA397842708 | TP53 | c.412G>T (p.Ala138Ser) c.16G>T (p.Ala6Ser) c.133G>T (p.Ala45Ser) c.391G>T (p.Ala131Ser) n.668G>T c.295G>T (p.Ala99Ser) c.-66G>T (n.-66G>T) c.379G>T (p.Ala127Ser) | dbSNP COSMIC |
17 | g.7675200C>T | CA397842713 | TP53 | c.412G>A (p.Ala138Thr) c.16G>A (p.Ala6Thr) c.133G>A (p.Ala45Thr) c.391G>A (p.Ala131Thr) n.668G>A c.295G>A (p.Ala99Thr) c.-66G>A (n.-66G>A) c.379G>A (p.Ala127Thr) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |