|
CFTR-NGS variants catalogue
Variant hg19:chr7:117188682G/T
| Name | NM_000492.4:c.1210-13G>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117188682G>T UCSC gnomAD |
| #Exon/intron | intron 9 |
| Legacy Name | TG10T9 |
| Type in CFTR-NGS catalogue | TG-T |
| Class in CFTR-France | non disease-causing |
| Patients reported in CFTR-NGS, carrying this variant also carry: |