|
CFTR-NGS variants catalogue
Variant hg19:chr7:117277554A/T
| Name | NM_000492.4:c.3718-4938A>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117277554A>T UCSC gnomAD |
| #Exon/intron | intron 22 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| Patients reported in CFTR-NGS, carrying this variant also carry: |