Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673824C>T | CA397837142 | TP53 | c.796G>A (p.Gly266Arg) c.400G>A (p.Gly134Arg) c.517G>A (p.Gly173Arg) c.775G>A (p.Gly259Arg) c.782+357G>A (n.782+357G>A) c.679G>A (p.Gly227Arg) c.319G>A (p.Gly107Arg) c.763G>A (p.Gly255Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673824C>G | CA16603026 | TP53 | c.796G>C (p.Gly266Arg) c.400G>C (p.Gly134Arg) c.517G>C (p.Gly173Arg) c.775G>C (p.Gly259Arg) c.782+357G>C (n.782+357G>C) c.679G>C (p.Gly227Arg) c.319G>C (p.Gly107Arg) c.763G>C (p.Gly255Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673824C>A | CA397837139 | TP53 | c.796G>T (p.Gly266Ter) c.400G>T (p.Gly134Ter) c.517G>T (p.Gly173Ter) c.775G>T (p.Gly259Ter) c.782+357G>T (n.782+357G>T) c.679G>T (p.Gly227Ter) c.319G>T (p.Gly107Ter) c.763G>T (p.Gly255Ter) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC |