catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117186038A/AATTTT


CFTR-NGS Variant details:
Name NM_000492.4:c.1210-2636_1210-2632dup5
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117186059_117186063dup    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: