| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.55088939G>A | CA122126 | KDR | c.3439C>T (p.Pro1147Ser) n.3452C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.55088939G>C | CA356901489 | KDR | c.3439C>G (p.Pro1147Ala) n.3452C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.55088939G= | CA1458927152 | KDR | c.3439C= (p.Pro1147=) n.3452C= | dbSNP |