catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117276872C/CT


CFTR-NGS Variant details:
Name NM_000492.4:c.3718-5607dupT
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117276885dup    UCSC    
#Exon/intron intron 22
Type in CFTR-NGS catalogue repeat
Class in CFTR-France not reported
WT sequence AAAACCTTTAGCTTTTTTTTTTTTT - CTTTTTGAGGTGGAGTCTCACTGTT
Mutant sequence AAAACCTTTAGCTTTTTTTTTTTTT T CTTTTTGAGGTGGAGTCTCACTGTT


Additional information:
MAF (GnomAD) 7.39e-03
Splicing prediction (SpliceAI) AG: 0.00 (23)
AL: 0.00 (0)
DG: 0.00 (23)
DL: 0.00 (-31)




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


3 individuals (out of 136) carrying this variant are reported in CFTR-NGS catalogue:

TOTAL NUMBER OF INDIVIDUALS 3
Asymptomatic 2
CFTR-RD1
  • CFTR-RD  1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
MUCO07319AsymptomaticMontpellier100714_varilhheterozygous PASS 5880 153
m8583AsymptomaticMontpellier150419_Altieriheterozygous PASS 186 75
5CFTR-RDMontpellier150517_varilhheterozygous PASS 2003 344





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