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CFTR-NGS variants catalogue
Variant hg19:chr7:117187003C/T
| Name | NM_000492.4:c.1210-1692C>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117187003C>T UCSC gnomAD |
| #Exon/intron | intron 9 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | TTGGTTGTTCTCTTGAATGTACTGC C ATATGACGTGGTGTGATTTCAATTG |
| Mutant sequence | TTGGTTGTTCTCTTGAATGTACTGC T ATATGACGTGGTGTGATTTCAATTG |
| MAF (GnomAD) | 6.49e-03 |
| Splicing prediction (SpliceAI) | AG: 0.00 (-31) AL: 0.00 (-25) DG: 0.00 (-31) DL: 0.00 (-8) |
 Not found |  Not found | dbSNP rs144014422 |  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 |
|---|---|---|---|---|---|---|---|
| 9878 | Asymptomatic | Montpellier | 160218_varilh | heterozygous | PASS | 2387 | 256 |
| P6Cr | Suspicion of CF | Montpellier | 230414_varilh | heterozygous | PASS | 9457 | 698 |
