| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.101428468C>A | CA5161643 | ALDOB | c.379+1G>T (n.379+1G>T) n.67+1341G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.101428468C>T | CA16041287 | ALDOB | c.379+1G>A (n.379+1G>A) n.67+1341G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.101428468C= | CA1868280499 | ALDOB | c.379+1G= (n.379+1G=) n.67+1341G= | dbSNP |