Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.15189004A>G | CA340888 | NOTCH3 | c.1363T>C (p.Cys455Arg) c.1360T>C (p.Cys454Arg) | ClinVar dbSNP |
19 | g.15189004A>T | CA404527578 | NOTCH3 | c.1363T>A (p.Cys455Ser) c.1360T>A (p.Cys454Ser) | ClinVar dbSNP |
19 | g.15189004A= | CA2324748606 | NOTCH3 | c.1363T= (p.Cys455=) c.1360T= (p.Cys454=) | dbSNP |