Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.47881800C>A | CA14677499 | SULT2A1 | c.472+284G>T (n.472+284G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.47881800C>G | CA2339629879 | SULT2A1 | c.472+284G>C (n.472+284G>C) | dbSNP |
19 | g.47881800C>T | CA2339629880 | SULT2A1 | c.472+284G>A (n.472+284G>A) | dbSNP |