| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.55113391C>T | CA160337 | KDR | c.889G>A (p.Val297Ile) n.902G>A n.889G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.55113391C>A | CA356914955 | KDR | c.889G>T (p.Val297Leu) n.902G>T n.889G>T | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.55113391C= | CA1458933822 | KDR | c.889G= (p.Val297=) n.902G= n.889G= | dbSNP |