| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.180616464C>G | CA257465 | FLT4 | c.3122G>C (p.Arg1041Pro) n.2515G>C c.236G>C (p.Arg79Pro) n.489G>C c.*2065G>C (n.*2065G>C) c.3371G>C (p.Arg1124Pro) c.3353G>C (p.Arg1118Pro) c.3140G>C (p.Arg1047Pro) c.3062G>C (p.Arg1021Pro) c.2663G>C (p.Arg888Pro) n.3383G>C c.3044G>C (p.Arg1015Pro) n.3587G>C | ClinVar dbSNP |
| 5 | g.180616464C>T | CA362500581 | FLT4 | c.3122G>A (p.Arg1041Gln) n.2515G>A c.236G>A (p.Arg79Gln) n.489G>A c.*2065G>A (n.*2065G>A) c.3371G>A (p.Arg1124Gln) c.3353G>A (p.Arg1118Gln) c.3140G>A (p.Arg1047Gln) c.3062G>A (p.Arg1021Gln) c.2663G>A (p.Arg888Gln) n.3383G>A c.3044G>A (p.Arg1015Gln) n.3587G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |