catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117188682G/GTT


CFTR-NGS Variant details:
Name NM_000492.4:c.1210-7_1210-6dupTT
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117188688_117188689dup    UCSC    
#Exon/intron intron 9
Legacy Name TG11T9
Type in CFTR-NGS catalogue TG-T
Class in CFTR-France non disease-causing
WT sequence TGTGTGTGTGTGTGTGTGTTTTTTT -- AACAGGGATTTGGGGAATTATTTGA
Mutant sequence TGTGTGTGTGTGTGTGTGTTTTTTT TT AACAGGGATTTGGGGAATTATTTGA


Additional information:
MAF (GnomAD) 4.53e-02
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
9CFTR-RDMontpellier150517_varilhheterozygous PASS 3913 549





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