Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673552C>G | CA397835806 | TP53 | c.976G>C (p.Glu326Gln) c.580G>C (p.Glu194Gln) c.697G>C (p.Glu233Gln) c.955G>C (p.Glu319Gln) c.782+629G>C (n.782+629G>C) c.36G>C c.859G>C (p.Glu287Gln) c.499G>C (p.Glu167Gln) c.943G>C (p.Glu315Gln) | dbSNP |
17 | g.7673552C>T | CA397835809 | TP53 | c.976G>A (p.Glu326Lys) c.580G>A (p.Glu194Lys) c.697G>A (p.Glu233Lys) c.955G>A (p.Glu319Lys) c.782+629G>A (n.782+629G>A) c.36G>A c.859G>A (p.Glu287Lys) c.499G>A (p.Glu167Lys) c.943G>A (p.Glu315Lys) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673552C>A | CA10580908 | TP53 | c.976G>T (p.Glu326Ter) c.580G>T (p.Glu194Ter) c.697G>T (p.Glu233Ter) c.955G>T (p.Glu319Ter) c.782+629G>T (n.782+629G>T) c.36G>T c.859G>T (p.Glu287Ter) c.499G>T (p.Glu167Ter) c.943G>T (p.Glu315Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |