catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3196C>T
Protein name NP_000483.3:p.(Arg1066Cys)
Genomic name (hg19) chr7:g.117251691C>T    UCSC    gnomAD
#Exon/intron exon 20
Legacy Name R1066C
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence AAGCTTAAAAGGACTATGGACACTT C GTGCCTTCGGACGGCAGCCTTACTT
Mutant sequence AAGCTTAAAAGGACTATGGACACTT T GTGCCTTCGGACGGCAGCCTTACTT


Additional information:
MAF (GnomAD) -
Splicing prediction (SpliceAI) -

External sources:
dbSNP
no rs

Variant validation:
Sanger
(present/not present/not verified)
Minigene
(effect/no effect/not performed)
present not performed


Pathogenicity predictions:
AGVGD MAPP SIFT PPH2
C35 0.00014 0 1
VUS2 VUS5 VUS5 VUS5
Color code:   non disease-causing <   VUS1 <   VUS2 <   VUS3 <   VUS4 <   VUS5 <   disease-causing


No patient found in CFTR-NGS

20 individuals reported in CFTR-France







Go to CFTRare
VLMCHUUM