Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.55087316G>A | CA11687978 | KDR | c.3662+291C>T (n.3662+291C>T) n.3675+291C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.55087316G>C | CA1458926492 | KDR | c.3662+291C>G (n.3662+291C>G) n.3675+291C>G | dbSNP |
4 | g.55087316G>T | CA2580589101 | KDR | c.3662+291C>A (n.3662+291C>A) n.3675+291C>A | dbSNP |
4 | g.55087316G= | CA1458926491 | KDR | c.3662+291C= (n.3662+291C=) n.3675+291C= | dbSNP |