| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.232539760C>T | CA128047 | CHRNG | c.13C>T (p.Gln5Ter) n.34C>T | ClinVar dbSNP |
| 2 | g.232539760C= | CA1335312144 | CHRNG | c.13C= (p.Gln5=) n.34C= | dbSNP |
| 2 | g.232539760C>A | CA351006734 | CHRNG | c.13C>A (p.Gln5Lys) n.34C>A | dbSNP gnomAD v4 |