| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.102701594G>T | CA102713539 | MANBA | c.674-10823C>A (n.674-10823C>A) c.180-10823C>A c.356-10823C>A (n.356-10823C>A) c.503-10823C>A (n.503-10823C>A) n.721-10637C>A c.311-10823C>A (n.311-10823C>A) c.26-10823C>A (n.26-10823C>A) c.599-10823C>A (n.599-10823C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.102701594G>C | CA1481487228 | MANBA | c.674-10823C>G (n.674-10823C>G) c.180-10823C>G c.356-10823C>G (n.356-10823C>G) c.503-10823C>G (n.503-10823C>G) n.721-10637C>G c.311-10823C>G (n.311-10823C>G) c.26-10823C>G (n.26-10823C>G) c.599-10823C>G (n.599-10823C>G) | dbSNP |