catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117220096GAAGAAAAAAAGATAGCAAACAAAT/G


CFTR-NGS Variant details:
Name NM_000492.4:c.1585-7695_1585-7670del26
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117220098_117220123del    UCSC    
#Exon/intron intron 11
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence GGAATTTTTCACTTGAAATACTAGA AGAAAA [14bp] AATACA GGAATTCCAATTTCAAGCAGATATA
Mutant sequence GGAATTTTTCACTTGAAATACTAGA -------------------- GGAATTCCAATTTCAAGCAGATATA


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
Pending (NBS) 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
3190Pending (NBS)Montpellier40216_varilhheterozygous alleleBias 53 0





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