catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117206302A/AACACACAC


CFTR-NGS Variant details:
Name NM_000492.4:c.1584+6624_1584+6631dup8
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117206333_117206340dup    UCSC    
#Exon/intron intron 11
Type in CFTR-NGS catalogue microsatellite
Class in CFTR-France not reported
WT sequence CACACACACACACACACACACACAC -------- TAGCCAGGCGTGGTGGTGCACGTTT
Mutant sequence CACACACACACACACACACACACAC ACACACAC TAGCCAGGCGTGGTGGTGCACGTTT


Additional information:
MAF (GnomAD) 3.26e-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


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

TOTAL NUMBER OF INDIVIDUALS 3
Asymptomatic 3



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
m2762AsymptomaticMontpellier230414_varilhheterozygous PASS 10380 179
MUCO07381AsymptomaticMontpellier100714_varilhhomozygous alleleBias 182 0
m9946AsymptomaticMontpellier150419_Altieriheterozygous PASS 147 47





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