catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117144916A/AT


CFTR-NGS Variant details:
Name NM_000492.4:c.164+507dupT
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117144924dup    UCSC    
#Exon/intron intron 2
Type in CFTR-NGS catalogue repeat
Class in CFTR-France not reported
WT sequence AGTTTCCTAAGAAATGATTTTTTTT - CCTGAAAAATACACATTTGGTTTCA
Mutant sequence AGTTTCCTAAGAAATGATTTTTTTT T CCTGAAAAATACACATTTGGTTTCA


Additional information:
MAF (GnomAD) 1.17e-02
Splicing prediction (SpliceAI) AG: 0.00 (35)
AL: 0.00 (37)
DG: 0.00 (37)
DL: 0.00 (16)




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


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

TOTAL NUMBER OF INDIVIDUALS 4
Asymptomatic 1
CF 1
CFTR-RD2
  • CFTR-RD  2



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
MUCO07318AsymptomaticMontpellier100714_varilhheterozygous PASS 825 37
9777CFMontpellier160218_varilhheterozygous PASS 2469 258
6959CFTR-RDMontpellier40216_varilhheterozygous PASS 860 90
m8107CFTR-RDMontpellier150419_Altieriheterozygous PASS 268 45





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