| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.117614713G>T | CA4451462 | CFTR | c.3468G>T (p.Leu1156Phe) c.*3182G>T (n.*3182G>T) c.3285G>T (p.Leu1095Phe) c.*1843G>T (n.*1843G>T) c.3462G>T (p.Leu1154Phe) c.*3292G>T (n.*3292G>T) c.3042G>T (p.Leu1014Phe) c.216G>T (p.Leu72Phe) c.1059G>T (p.Leu353Phe) c.50G>T c.1118G>T c.2250G>T (p.Leu750Phe) c.3378G>T (p.Leu1126Phe) c.293G>T c.3558G>T (p.Leu1186Phe) c.3225G>T (p.Leu1075Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.117614713G>A | CA242034 | CFTR | c.3468G>A (p.Leu1156=) c.*3182G>A (n.*3182G>A) c.3285G>A (p.Leu1095=) c.*1843G>A (n.*1843G>A) c.3462G>A (p.Leu1154=) c.*3292G>A (n.*3292G>A) c.3042G>A (p.Leu1014=) c.216G>A (p.Leu72=) c.1059G>A (p.Leu353=) c.50G>A c.1118G>A c.2250G>A (p.Leu750=) c.3378G>A (p.Leu1126=) c.293G>A c.3558G>A (p.Leu1186=) c.3225G>A (p.Leu1075=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |