catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117192683TCCTGCATTC/C


CFTR-NGS Variant details:
Name NM_000492.4:c.1392+3810_1392+3818del9
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117192687_117192695del    UCSC    
#Exon/intron intron 10
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence TCATCTGTCCATTTTCCATTCTCCT GCATTCCCT CATCCAACCAAGGTAGCCAATCCAG
Mutant sequence TCATCTGTCCATTTTCCATTCTCCT --------- CATCCAACCAAGGTAGCCAATCCAG


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
CFTR-RD1
  • CFTR-RD  1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
8442CFTR-RDMontpellier40216_varilhheterozygous alleleBias 40 0





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