| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.23631056A>G | CA15798901 | TNFRSF19 | c.445+4264A>G (n.445+4264A>G) c.49+4264A>G (n.49+4264A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.23631056A>T | CA2078774942 | TNFRSF19 | c.445+4264A>T (n.445+4264A>T) c.49+4264A>T (n.49+4264A>T) | dbSNP |