Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.28018500G>T | CA483042234 | FLT3 | c.2508C>A (p.Ile836=) c.*420C>A (n.*420C>A) n.2722C>A c.2451C>A (p.Ile817=) c.1983C>A (p.Ile661=) c.2292C>A (p.Ile764=) c.1629C>A (p.Ile543=) c.1611C>A (p.Ile537=) n.2706C>A | dbSNP COSMIC |
13 | g.28018500G>A | CA483042233 | FLT3 | c.2508C>T (p.Ile836=) c.*420C>T (n.*420C>T) n.2722C>T c.2451C>T (p.Ile817=) c.1983C>T (p.Ile661=) c.2292C>T (p.Ile764=) c.1629C>T (p.Ile543=) c.1611C>T (p.Ile537=) n.2706C>T | dbSNP |
13 | g.28018500G>C | CA16602446 | FLT3 | c.2508C>G (p.Ile836Met) c.*420C>G (n.*420C>G) n.2722C>G c.2451C>G (p.Ile817Met) c.1983C>G (p.Ile661Met) c.2292C>G (p.Ile764Met) c.1629C>G (p.Ile543Met) c.1611C>G (p.Ile537Met) n.2706C>G | ClinVar dbSNP COSMIC |