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CFTR-NGS variants catalogue
Variant hg19:chr7:117150904C/A
| Name | NM_000492.4:c.273+1708C>A |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117150904C>A UCSC gnomAD |
| #Exon/intron | intron 3 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | CCAGTTCAATATGAAGGTCTTTATG C AGATTATTTTACTTAATTTTCCTAG |
| Mutant sequence | CCAGTTCAATATGAAGGTCTTTATG A AGATTATTTTACTTAATTTTCCTAG |
| MAF (GnomAD) | 1.90e-02 |
| Splicing prediction (SpliceAI) | AG: 0.00 (26) AL: 0.00 (3) DG: 0.00 (24) DL: 0.00 (-10) |
 Not found |  Not found | dbSNP rs77074965 |  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 | 4 |
|---|---|
| Asymptomatic | 2 |
| Pending (NBS) | 1 |
| Suspicion of CF | 1 |
| ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
|---|---|---|---|---|---|---|---|
| MUCO07299 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 3034 | 281 |
| T17 | Asymptomatic | Montpellier | 160218_varilh | heterozygous | PASS | 4216 | 328 |
| 1 | Pending (NBS) | Montpellier | 150517_varilh | heterozygous | PASS | 5666 | 472 |
| m8852 | Suspicion of CF | Montpellier | 150419_Altieri | heterozygous | PASS | 762 | 121 |
