Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7676211C>T | CA10580959 | TP53 | c.158G>A (p.Trp53Ter) c.-21-975G>A (n.-21-975G>A) c.96+171G>A (n.96+171G>A) n.414G>A c.41G>A (p.Trp14Ter) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676211C>G | CA397846478 | TP53 | c.158G>C (p.Trp53Ser) c.-21-975G>C (n.-21-975G>C) c.96+171G>C (n.96+171G>C) n.414G>C c.41G>C (p.Trp14Ser) | dbSNP |
17 | g.7676211C>A | CA397846483 | TP53 | c.158G>T (p.Trp53Leu) c.-21-975G>T (n.-21-975G>T) c.96+171G>T (n.96+171G>T) n.414G>T c.41G>T (p.Trp14Leu) | ClinVar dbSNP |