| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.111757172T>A | CA2063467528 | c.104+1427T>A c.99+1427T>A (n.99+1427T>A) | dbSNP gnomAD v4 | |
| 12 | g.111757172T>C | CA13632868 | c.104+1427T>C c.99+1427T>C (n.99+1427T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 12 | g.111757172T>G | CA2063467529 | c.104+1427T>G c.99+1427T>G (n.99+1427T>G) | dbSNP |