| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.191075725G>T | CA762406525 | STAT4 | c.372+502C>A (n.372+502C>A) n.440+502C>A c.399+502C>A (n.399+502C>A) | dbSNP |
| 2 | g.191075725G>C | CA1316316452 | STAT4 | c.372+502C>G (n.372+502C>G) n.440+502C>G c.399+502C>G (n.399+502C>G) | dbSNP |
| 2 | g.191075725G>A | CA15155278 | STAT4 | c.372+502C>T (n.372+502C>T) n.440+502C>T c.399+502C>T (n.399+502C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |