catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117289331GAT/G


CFTR-NGS Variant details:
Name NM_000492.4:c.3874-3564_3874-3563delAT
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117289332_117289333del    UCSC    
#Exon/intron intron 23
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence ACATTTTAATAGAATTATACATGGG AT GTGTGTGTGTGTGTGTGTGTGTGTA
Mutant sequence ACATTTTAATAGAATTATACATGGG -- GTGTGTGTGTGTGTGTGTGTGTGTA


Additional information:
MAF (GnomAD) 0.00e+00
Splicing prediction (SpliceAI) AG: 0.00 (-50)
AL: 0.00 (29)
DG: 0.00 (0)
DL: 0.00 (-12)




External sources:

Not found

Not found
dbSNP
rs67557270

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


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

TOTAL NUMBER OF INDIVIDUALS 8
Asymptomatic 3
CF 3
CFTR-RD1
  • CFTR-RD  1
Suspicion of CF 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
m5062AsymptomaticMontpellier230414_varilhheterozygous PASS 1256 275
m93AsymptomaticMontpellier230414_varilhheterozygous PASS 128 47
T18AsymptomaticMontpellier160218_varilhheterozygous PASS 712 84
m2760CFMontpellier230414_varilhheterozygous LowVariantFreq 706 256
m6426CFMontpellier230414_varilhheterozygous PASS 925 168
P1BCFMontpellier230414_varilhheterozygous PASS 1173 340
P1CoCFTR-RDMontpellier230414_varilhheterozygous PASS 2387 450
m9196Suspicion of CFMontpellier150419_Altieriheterozygous PASS 64 24





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