| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.101421891G>A | CA199050 | ALDOB | c.1013C>T (p.Ala338Val) c.*25C>T (n.*25C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.101421891G>T | CA374264110 | ALDOB | c.1013C>A (p.Ala338Glu) c.*25C>A (n.*25C>A) | dbSNP gnomAD v4 |
| 9 | g.101421891G>C | CA5161399 | ALDOB | c.1013C>G (p.Ala338Gly) c.*25C>G (n.*25C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |