Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.28018502T>C | CA16603129 | FLT3 | c.2506A>G (p.Ile836Val) c.*418A>G (n.*418A>G) n.2720A>G c.2449A>G (p.Ile817Val) c.1981A>G (p.Ile661Val) c.2290A>G (p.Ile764Val) c.1627A>G (p.Ile543Val) c.1609A>G (p.Ile537Val) n.2704A>G | ClinVar dbSNP |
13 | g.28018502T>G | CA16602447 | FLT3 | c.2506A>C (p.Ile836Leu) c.*418A>C (n.*418A>C) n.2720A>C c.2449A>C (p.Ile817Leu) c.1981A>C (p.Ile661Leu) c.2290A>C (p.Ile764Leu) c.1627A>C (p.Ile543Leu) c.1609A>C (p.Ile537Leu) n.2704A>C | ClinVar dbSNP COSMIC |
13 | g.28018502T>A | CA16603131 | FLT3 | c.2506A>T (p.Ile836Phe) c.*418A>T (n.*418A>T) n.2720A>T c.2449A>T (p.Ile817Phe) c.1981A>T (p.Ile661Phe) c.2290A>T (p.Ile764Phe) c.1627A>T (p.Ile543Phe) c.1609A>T (p.Ile537Phe) n.2704A>T | ClinVar dbSNP |