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CFTR-NGS variants catalogue
Variant hg19:chr7:117120775T/G
| Name | NM_000492.4:c.53+574T>G |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117120775T>G UCSC gnomAD |
| #Exon/intron | intron 1 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | GAAAGCAAATTTGTTGAAATATTTA T TTTGAAAAAAGTTACTTCACAAGCT |
| Mutant sequence | GAAAGCAAATTTGTTGAAATATTTA G TTTGAAAAAAGTTACTTCACAAGCT |
| MAF (GnomAD) | 2.04e-02 |
| Splicing prediction (SpliceAI) | AG: 0.00 (1) AL: 0.00 (-46) DG: 0.00 (-47) DL: 0.00 (-49) |
 Not found |  Not found | dbSNP rs35091062 |  Not found |  |
| Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
| present | 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 |
|---|---|---|---|---|---|---|---|
| 9 | CFTR-RD | Montpellier | 150517_varilh | heterozygous | PASS | 6667 | 514 |
