|
CFTR-NGS variants catalogue
Variant hg19:chr7:117199457A/G
| Name | NM_000492.4:c.1393-61A>G |
| Protein name | NP_000483.3:p.(=) |
| Genomic name (hg19) | chr7:g.117199457A>G UCSC gnomAD |
| #Exon/intron | intron 10 |
| Legacy Name | 1525-61A/G |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | non disease-causing |
| Patients reported in CFTR-NGS, carrying this variant also carry: |