catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117169601T/A


CFTR-NGS Variant details:
Name NM_000492.4:c.274-1352T>A
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117169601T>A    UCSC    gnomAD
#Exon/intron intron 3
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
Patients reported in CFTR-NGS, carrying this variant also carry: