catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117293054A/T


CFTR-NGS Variant details:
Name NM_000492.4:c.3963+69A>G
Protein name NP_000483.3:p.(=)
Genomic name (hg19) chr7:g.117293054A>G    UCSC    gnomAD
#Exon/intron intron 24
Type in CFTR-NGS catalogue -
Class in CFTR-France non disease-causing
WT sequence CCAACACAAATGGCTGATATAGCTG A CATCATTCTACACACTTTGTGTGCA
Mutant sequence CCAACACAAATGGCTGATATAGCTG G CATCATTCTACACACTTTGTGTGCA


Additional information:
MAF (GnomAD) -
Splicing prediction (SpliceAI) AG: 0.00 (41)
AL: 0.00 (12)
DG: 0.00 (-36)
DL: 0.00 (26)




External sources:

Not found		dbSNP
no rs
Not found

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



6 individuals carrying this variant are reported 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
3199CFTR-RDMontpellier40216_varilhheterozygous PASS 2783 248





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