|
CFTR-NGS variants catalogue
Variant hg19:chr7:117179986A/G
| Name | NM_000492.4:c.870-168A>G |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117179986A>G UCSC gnomAD |
| #Exon/intron | intron 7 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | TTCATATAAGGTAACTGAGGCCCAG A GAGATTAAATAACATGCCCAAGGTC |
| Mutant sequence | TTCATATAAGGTAACTGAGGCCCAG G GAGATTAAATAACATGCCCAAGGTC |
| MAF (GnomAD) | 1.74e-02 |
| Splicing prediction (SpliceAI) | AG: 0.00 (-45) AL: 0.00 (-15) DG: 0.00 (-16) DL: 0.00 (31) |
 Not found |  Not found | dbSNP rs115770955 |  Not found |  |
| Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
| not verified | not performed |
No patient found in CFTR-France |
| TOTAL NUMBER OF INDIVIDUALS | 2 |
|---|---|
| Asymptomatic | 1 |
| Suspicion of CF | 1 |
| ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
|---|---|---|---|---|---|---|---|
| MUCO07358 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 1575 | 93 |
| cad200291 | Suspicion of CF | Montpellier | 151220_Altieri | heterozygous | PASS | 1560 | 161 |
