|
CFTR-NGS variants catalogue
Variant hg19:chr7:117257871C/T
| Name | NM_000492.4:c.3468+3104C>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117257871C>T UCSC gnomAD |
| #Exon/intron | intron 21 |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | not reported |
| Patients reported in CFTR-NGS, carrying this variant also carry: |