| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.16940415G>A | CA8413957 | TNFRSF13B | c.542C>T (p.Ala181Val) n.648C>T c.446-7239C>T (n.446-7239C>T) n.350-7478C>T c.404C>T (p.Ala135Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16940415G>T | CA117389 | TNFRSF13B | c.542C>A (p.Ala181Glu) n.648C>A c.446-7239C>A (n.446-7239C>A) n.350-7478C>A c.404C>A (p.Ala135Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |