Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.100825743T>C | CA12476873 | EPHB4 | c.52+1236A>G (n.52+1236A>G) n.52+1236A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.100825743T>G | CA1729513850 | EPHB4 | c.52+1236A>C (n.52+1236A>C) n.52+1236A>C | dbSNP |
7 | g.100825743T>A | CA1729513849 | EPHB4 | c.52+1236A>T (n.52+1236A>T) n.52+1236A>T | dbSNP |