|
CFTR-NGS variants catalogue
Variant hg19:chr7:117296451C/T
| Name | NM_000492.4:c.3963+3466C>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117296451C>T UCSC gnomAD |
| #Exon/intron | intron 24 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | TTGGGTATGTGGCTGTGAGCACTGC C GGGCAAAATGCCATATGACCTAGAT |
| Mutant sequence | TTGGGTATGTGGCTGTGAGCACTGC T GGGCAAAATGCCATATGACCTAGAT |
| MAF (GnomAD) | 4.68e-04 |
| Splicing prediction (SpliceAI) | AG: 0.00 (49) AL: 0.00 (-45) DG: 0.00 (-22) DL: 0.00 (30) |
 Not found |  Not found | dbSNP rs184714132 |  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 | 1 |
|---|---|
| CFTR-RD | 1
|
| ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
|---|---|---|---|---|---|---|---|
| 17MU00956 | CFTR-RD | Cochin | 150419_Altieri | heterozygous | PASS | 5756 | 439 |
