| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.56042170G>A | CA253780 | RPS26 | c.3+1G>A (n.3+1G>A) n.30+1G>A | ClinVar dbSNP |
| 12 | g.56042170G>T | CA385326242 | RPS26 | c.3+1G>T (n.3+1G>T) n.30+1G>T | ClinVar dbSNP |
| 12 | g.56042170G= | CA2038229738 | RPS26 | c.3+1G= (n.3+1G=) n.30+1G= | dbSNP |