catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117281194GTTCTTACGA/G


CFTR-NGS Variant details:
Name NM_000492.4:c.3718-1296_3718-1288del9
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117281196_117281204del    UCSC    
#Exon/intron intron 22
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence ATTTGTGAAAATCTCATTGTAGAGT TCTTACGAT GGATAGGGGGTCAACTGTGTCATTA
Mutant sequence ATTTGTGAAAATCTCATTGTAGAGT --------- GGATAGGGGGTCAACTGTGTCATTA


Additional information:
MAF (GnomAD) -
Splicing prediction (SpliceAI) -




External sources:

Not found
Not found		dbSNP
no rs
Not found

Variant validation:
Sanger
(present/not present/not verified)
 Minigene
(effect/no effect/not performed)
not verifiednot performed



No patient found in CFTR-France


1 individual (out of 136) carrying this variant is reported in CFTR-NGS catalogue:

TOTAL NUMBER OF INDIVIDUALS 1
CF 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
m2760CFMontpellier230414_varilhheterozygous alleleBias 220 0





Go to CFTRare
VLMCHUUM