| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.72012256G>C | CA668114700 | CHST3 | c.*3785G>C (n.*3785G>C) | dbSNP |
| 10 | g.72012256G>T | CA668114696 | CHST3 | c.*3785G>T (n.*3785G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.72012256G>A | CA10632140 | CHST3 | c.*3785G>A (n.*3785G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |