catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117218146C/T


CFTR-NGS Variant details:
Name NM_000492.4:c.1585-9647C>T
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117218146C>T    UCSC    gnomAD
#Exon/intron intron 11
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence ATGTGTATATACATGTACATATATG C ATGTATATTCAATTGTATATGTGTA
Mutant sequence ATGTGTATATACATGTACATATATG T ATGTATATTCAATTGTATATGTGTA


Additional information:
MAF (GnomAD) 1.40e-02
Splicing prediction (SpliceAI) AG: 0.00 (-2)
AL: 0.00 (47)
DG: 0.00 (-2)
DL: 0.00 (2)




External sources:

Not found
Not found		dbSNP
rs80079539
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
3641CFTR-RDMontpellier40216_varilhheterozygous PASS 523 40





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