| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.151627231G>A | CA170719 | n.657G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 6 | g.151627231G= | CA1672973859 | n.657G= | dbSNP | |
| 6 | g.151627231G>C | CA2580575610 | n.657G>C | dbSNP | |
| 6 | g.151627231G>T | CA2580575611 | n.657G>T | dbSNP |