| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.116655150C>A | CA2002674486 | LINC02702 | n.272+2097C>A n.371C>A | dbSNP |
| 11 | g.116655150C>T | CA230126502 | LINC02702 | n.272+2097C>T n.371C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116655150C= | CA2002674487 | LINC02702 | n.272+2097C= n.371C= | dbSNP |