catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117262636AAGTCTCTTTAT/T


CFTR-NGS Variant details:
Name NM_000492.4:c.3469-4936_3469-4926del11
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117262640_117262650del    UCSC    
#Exon/intron intron 21
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence CTTCTATAACTATCAGTTATGAAGT CTCTTTATAGT GTTGCCAGCCAGGTCTCAGGTGTGT
Mutant sequence CTTCTATAACTATCAGTTATGAAGT ----------- GTTGCCAGCCAGGTCTCAGGTGTGT


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
Asymptomatic 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
MUCO07299AsymptomaticMontpellier100714_varilhheterozygous alleleBias 53 0





Go to CFTRare
VLMCHUUM