CFTR-NGS variants catalogue
Variant hg19:chr7:117198607C/CTAAATAAA
Name | NM_000492.4:c.1393-882_1393-875dup8 |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117198636_117198643dup UCSC |
#Exon/intron | intron 10 |
Type in CFTR-NGS catalogue | microsatellite |
Class in CFTR-France | not reported |
Patients reported in CFTR-NGS, carrying this variant also carry: |