| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.117592292C>G | CA368979863 | CFTR | c.2125C>G (p.Arg709Gly) c.*1839C>G (n.*1839C>G) c.1942C>G (p.Arg648Gly) c.*425C>G (n.*425C>G) c.*1949C>G (n.*1949C>G) c.1699C>G (p.Arg567Gly) c.1402-10534C>G (n.1402-10534C>G) c.2035C>G (p.Arg679Gly) c.2215C>G (p.Arg739Gly) c.1882C>G (p.Arg628Gly) | ClinVar dbSNP gnomAD v4 |
| 7 | g.117592292C>T | CA328093 | CFTR | c.2125C>T (p.Arg709Ter) c.*1839C>T (n.*1839C>T) c.1942C>T (p.Arg648Ter) c.*425C>T (n.*425C>T) c.*1949C>T (n.*1949C>T) c.1699C>T (p.Arg567Ter) c.1402-10534C>T (n.1402-10534C>T) c.2035C>T (p.Arg679Ter) c.2215C>T (p.Arg739Ter) c.1882C>T (p.Arg628Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |