Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7676210C>G | CA397846446 | TP53 | c.159G>C (p.Trp53Cys) c.-21-974G>C (n.-21-974G>C) c.96+172G>C (n.96+172G>C) n.415G>C c.42G>C (p.Trp14Cys) | dbSNP COSMIC |
17 | g.7676210C>T | CA16620640 | TP53 | c.159G>A (p.Trp53Ter) c.-21-974G>A (n.-21-974G>A) c.96+172G>A (n.96+172G>A) n.415G>A c.42G>A (p.Trp14Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676210C>A | CA397846443 | TP53 | c.159G>T (p.Trp53Cys) c.-21-974G>T (n.-21-974G>T) c.96+172G>T (n.96+172G>T) n.415G>T c.42G>T (p.Trp14Cys) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |