| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.58899597G>T | CA262063232 | LINC01500 | n.457+5266G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.58899597G>C | CA2140112667 | LINC01500 | n.457+5266G>C | dbSNP |
| 14 | g.58899597G>A | CA707238792 | LINC01500 | n.457+5266G>A | dbSNP gnomAD v3 gnomAD v4 |