Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.55091556A>G | CA11863161 | KDR | c.3069+1061T>C (n.3069+1061T>C) n.3082+1061T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.55091556A= | CA1458928293 | KDR | c.3069+1061T= (n.3069+1061T=) n.3082+1061T= | dbSNP |