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CFTR-NGS variants catalogue
| Name | NM_000492.4:c.2988+1616_3367+356del3796ins62 |
| Protein name | NP_000483.3:p.? |
| Genomic name (hg19) | chr7:g.117248423_117252218delins62 UCSC |
| #Exon/intron | intron 18 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | disease-causing |
| WT sequence | ACAGGCGCGCACCACCATGCCTGGA TAATTT [3784bp] CATACT-- CATATTGGTGAAGGGTCCTAGCTTC |
| Mutant sequence | ACAGGCGCGCACCACCATGCCTGGA CAAACC [50bp] TAATCC CATATTGGTGAAGGGTCCTAGCTTC |
| MAF (GnomAD) | - |
| Splicing prediction (SpliceAI) | - |
 Not found |  Not found | dbSNP no rs |  Not found |  Not found |
| Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
| present | not performed |
No patient found in CFTR-NGS |
No patient found in CFTR-France |
