| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.180613101G>A | CA257467 | FLT4 | c.3341C>T (p.Pro1114Leu) n.3691C>T n.293C>T c.*2284C>T (n.*2284C>T) c.3590C>T (p.Pro1197Leu) c.3572C>T (p.Pro1191Leu) c.3359C>T (p.Pro1120Leu) c.3281C>T (p.Pro1094Leu) c.2882C>T (p.Pro961Leu) n.3602C>T c.3263C>T (p.Pro1088Leu) n.3806C>T | ClinVar dbSNP COSMIC COSMIC |
| 5 | g.180613101G= | CA1604719167 | FLT4 | c.3341C= (p.Pro1114=) n.3691C= n.293C= c.*2284C= (n.*2284C=) c.3590C= (p.Pro1197=) c.3572C= (p.Pro1191=) c.3359C= (p.Pro1120=) c.3281C= (p.Pro1094=) c.2882C= (p.Pro961=) n.3602C= c.3263C= (p.Pro1088=) n.3806C= | dbSNP |