|
CFTR-NGS variants catalogue
Variant hg19:chr7:117188387GGT/G
| Name | NM_000492.4:c.1210-277_1210-276delGT |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117188418_117188419del UCSC |
| #Exon/intron | intron 9 |
| Type in CFTR-NGS catalogue | microsatellite |
| Class in CFTR-France | not reported |
| Patients reported in CFTR-NGS, carrying this variant also carry: |