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CFTR-NGS variants catalogue
Variant hg19:chr7:117145102T/C
| Name | NM_000492.4:c.164+685T>C |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117145102T>C UCSC gnomAD |
| #Exon/intron | intron 2 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| WT sequence | GTCTTAAGGTAATGGCTACTGGTTA T CAAACAAATGTAAAAATTGTATATT |
| Mutant sequence | GTCTTAAGGTAATGGCTACTGGTTA C CAAACAAATGTAAAAATTGTATATT |
| MAF (GnomAD) | 1.41e-02 |
| Splicing prediction (SpliceAI) | AG: 0.00 (9) AL: 0.00 (49) DG: 0.00 (9) DL: 0.00 (-18) |
 Not found |  Not found | dbSNP rs56296320 |  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 |
| CFTR-RD | 1
|
| ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
|---|---|---|---|---|---|---|---|
| MUCO07407 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 223 | 26 |
| 3641 | CFTR-RD | Montpellier | 40216_varilh | heterozygous | PASS | 1406 | 142 |
