Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673791A>C | CA397836909 | TP53 | c.829T>G (p.Cys277Gly) c.433T>G (p.Cys145Gly) c.550T>G (p.Cys184Gly) c.808T>G (p.Cys270Gly) c.782+390T>G (n.782+390T>G) c.712T>G (p.Cys238Gly) c.352T>G (p.Cys118Gly) c.796T>G (p.Cys266Gly) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673791A>T | CA397836911 | TP53 | c.829T>A (p.Cys277Ser) c.433T>A (p.Cys145Ser) c.550T>A (p.Cys184Ser) c.808T>A (p.Cys270Ser) c.782+390T>A (n.782+390T>A) c.712T>A (p.Cys238Ser) c.352T>A (p.Cys118Ser) c.796T>A (p.Cys266Ser) | dbSNP |
17 | g.7673791A>G | CA16620617 | TP53 | c.829T>C (p.Cys277Arg) c.433T>C (p.Cys145Arg) c.550T>C (p.Cys184Arg) c.808T>C (p.Cys270Arg) c.782+390T>C (n.782+390T>C) c.712T>C (p.Cys238Arg) c.352T>C (p.Cys118Arg) c.796T>C (p.Cys266Arg) | ClinVar dbSNP gnomAD v4 COSMIC |