| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.33153529G>T | CA13028770 | B4GALT1 | c.412+13229C>A (n.412+13229C>A) c.373+13229C>A (n.373+13229C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.33153529G>A | CA1844964818 | B4GALT1 | c.412+13229C>T (n.412+13229C>T) c.373+13229C>T (n.373+13229C>T) | dbSNP |