Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.28018501A>C | CA16603127 | FLT3 | c.2507T>G (p.Ile836Ser) c.*419T>G (n.*419T>G) n.2721T>G c.2450T>G (p.Ile817Ser) c.1982T>G (p.Ile661Ser) c.2291T>G (p.Ile764Ser) c.1628T>G (p.Ile543Ser) c.1610T>G (p.Ile537Ser) n.2705T>G | ClinVar dbSNP COSMIC |
13 | g.28018501A>T | CA387650199 | FLT3 | c.2507T>A (p.Ile836Asn) c.*419T>A (n.*419T>A) n.2721T>A c.2450T>A (p.Ile817Asn) c.1982T>A (p.Ile661Asn) c.2291T>A (p.Ile764Asn) c.1628T>A (p.Ile543Asn) c.1610T>A (p.Ile537Asn) n.2705T>A | dbSNP |
13 | g.28018501A>G | CA387650198 | FLT3 | c.2507T>C (p.Ile836Thr) c.*419T>C (n.*419T>C) n.2721T>C c.2450T>C (p.Ile817Thr) c.1982T>C (p.Ile661Thr) c.2291T>C (p.Ile764Thr) c.1628T>C (p.Ile543Thr) c.1610T>C (p.Ile537Thr) n.2705T>C | dbSNP COSMIC |