Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674200T>A | CA16603041 | TP53 | c.763A>T (p.Ile255Phe) c.367A>T (p.Ile123Phe) c.484A>T (p.Ile162Phe) c.742A>T (p.Ile248Phe) c.646A>T (p.Ile216Phe) c.286A>T (p.Ile96Phe) c.730A>T (p.Ile244Phe) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674200T= | CA2245951126 | TP53 | c.763A= (p.Ile255=) c.367A= (p.Ile123=) c.484A= (p.Ile162=) c.742A= (p.Ile248=) c.646A= (p.Ile216=) c.286A= (p.Ile96=) c.730A= (p.Ile244=) | dbSNP |