| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.55100634C>G | CA1458915551 | KDR | c.2266+1263G>C (n.2266+1263G>C) n.2279+1263G>C | dbSNP |
| 4 | g.55100634C>T | CA11687979 | KDR | c.2266+1263G>A (n.2266+1263G>A) n.2279+1263G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.55100634C= | CA1458915549 | KDR | c.2266+1263G= (n.2266+1263G=) n.2279+1263G= | dbSNP |