| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.232542288T>G | CA11140767 | CHRNG | c.507-135T>G (n.507-135T>G) c.351-135T>G (n.351-135T>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.232542288T>C | CA766143414 | CHRNG | c.507-135T>C (n.507-135T>C) c.351-135T>C (n.351-135T>C) | dbSNP gnomAD v4 |
| 2 | g.232542288T>A | CA1335317145 | CHRNG | c.507-135T>A (n.507-135T>A) c.351-135T>A (n.351-135T>A) | dbSNP |