| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.117559468C>G | CA342833 | CFTR,CFTR-AS1 | c.1397C>G (p.Ser466Ter) c.*1111C>G (n.*1111C>G) c.1214C>G (p.Ser405Ter) c.1392C>G (p.Phe464Leu) c.*1221C>G (n.*1221C>G) c.971C>G (p.Ser324Ter) c.1307C>G (p.Ser436Ter) c.1487C>G (p.Ser496Ter) c.1154C>G (p.Ser385Ter) n.221+1265G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.117559468C>A | CA328085 | CFTR,CFTR-AS1 | c.1397C>A (p.Ser466Ter) c.*1111C>A (n.*1111C>A) c.1214C>A (p.Ser405Ter) c.1392C>A (p.Phe464Leu) c.*1221C>A (n.*1221C>A) c.971C>A (p.Ser324Ter) c.1307C>A (p.Ser436Ter) c.1487C>A (p.Ser496Ter) c.1154C>A (p.Ser385Ter) n.221+1265G>T | ClinVar dbSNP gnomAD v4 |
| 7 | g.117559468C>T | CA326469 | CFTR,CFTR-AS1 | c.1397C>T (p.Ser466Leu) c.*1111C>T (n.*1111C>T) c.1214C>T (p.Ser405Leu) c.1392C>T (p.Phe464=) c.*1221C>T (n.*1221C>T) c.971C>T (p.Ser324Leu) c.1307C>T (p.Ser436Leu) c.1487C>T (p.Ser496Leu) c.1154C>T (p.Ser385Leu) n.221+1265G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |