Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.4683903G>A | CA12494942 | FOXK1 | c.560+1035G>A (n.560+1035G>A) c.71+8578G>A (n.71+8578G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.4683903G>C | CA153691887 | FOXK1 | c.560+1035G>C (n.560+1035G>C) c.71+8578G>C (n.71+8578G>C) | dbSNP |