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CFTR-NGS variants catalogue
Variant hg19:chr7:117199644ATCT/A
| Name | NM_000492.4:c.1521_1523del |
| Protein name | NP_000483.3:p.(Phe508del) |
| Genomic name (hg19) | chr7:g.117199646_117199648del UCSC |
| #Exon/intron | exon 11 |
| Legacy Name | ΔF508 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | disease-causing |
| Subclass | CF-causing |
| Patients reported in CFTR-NGS, carrying this variant also carry: |