| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.68157629C>T | CA13649226 | IFNG | c.366+284G>A (n.366+284G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.68157629C>A | CA2043752627 | IFNG | c.366+284G>T (n.366+284G>T) | dbSNP |
| 12 | g.68157629C= | CA2043752626 | IFNG | c.366+284G= (n.366+284G=) | dbSNP |