| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.180619344G>C | CA3606153 | FLT4 | c.2670C>G (p.His890Gln) n.2063C>G c.-128C>G (n.-128C>G) c.*1613C>G (n.*1613C>G) c.2919C>G (p.His973Gln) c.2901C>G (p.His967Gln) c.2688C>G (p.His896Gln) c.2610C>G (p.His870Gln) c.2211C>G (p.His737Gln) n.2931C>G c.2592C>G (p.His864Gln) n.3135C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.180619344G>T | CA362501605 | FLT4 | c.2670C>A (p.His890Gln) n.2063C>A c.-128C>A (n.-128C>A) c.*1613C>A (n.*1613C>A) c.2919C>A (p.His973Gln) c.2901C>A (p.His967Gln) c.2688C>A (p.His896Gln) c.2610C>A (p.His870Gln) c.2211C>A (p.His737Gln) n.2931C>A c.2592C>A (p.His864Gln) n.3135C>A | dbSNP gnomAD v4 |