| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.7929506C>A | CA520787188 | TNFRSF9 | c.679+3656G>T (n.679+3656G>T) c.223+3656G>T (n.223+3656G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.7929506C>T | CA10658701 | TNFRSF9 | c.679+3656G>A (n.679+3656G>A) c.223+3656G>A (n.223+3656G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |