| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.174221435T>C | CA11990036 | NSG2 | c.*18+16131T>C (n.*18+16131T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174221435T>G | CA1602103213 | NSG2 | c.*18+16131T>G (n.*18+16131T>G) | dbSNP |
| 5 | g.174221435T>A | CA807794449 | NSG2 | c.*18+16131T>A (n.*18+16131T>A) | dbSNP |