| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.117642451G>A | CA328120 | CFTR | c.3531G>A (p.Gly1177=) c.*3445G>A (n.*3445G>A) c.3548G>A (p.Gly1183Glu) c.3731G>A (p.Gly1244Glu) c.*384G>A (n.*384G>A) c.*392G>A (n.*392G>A) c.*2106G>A (n.*2106G>A) c.3725G>A (p.Gly1242Glu) c.*3555G>A (n.*3555G>A) c.3305G>A (p.Gly1102Glu) c.479G>A (p.Gly160Glu) c.1518G>A (n.1518G>A) c.313G>A c.1181G>A c.3641G>A (p.Gly1214Glu) c.3821G>A (p.Gly1274Glu) c.3488G>A (p.Gly1163Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.117642451G>T | CA327266 | CFTR | c.3531G>T (p.Gly1177=) c.*3445G>T (n.*3445G>T) c.3548G>T (p.Gly1183Val) c.3731G>T (p.Gly1244Val) c.*384G>T (n.*384G>T) c.*392G>T (n.*392G>T) c.*2106G>T (n.*2106G>T) c.3725G>T (p.Gly1242Val) c.*3555G>T (n.*3555G>T) c.3305G>T (p.Gly1102Val) c.479G>T (p.Gly160Val) c.1518G>T (n.1518G>T) c.313G>T c.1181G>T c.3641G>T (p.Gly1214Val) c.3821G>T (p.Gly1274Val) c.3488G>T (p.Gly1163Val) | ClinVar dbSNP |