catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.2052dup
Protein name NP_000483.3:p.(Gln685Thrfs*4)
Genomic name (hg19) chr7:g.117232273dup    UCSC    
#Exon/intron exon 14
Legacy Name 2184insA
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence TGTCTCCTGGACAGAAACAAAAAAA - CAATCTTTTAAACAGACTGGAGAGT
Mutant sequence TGTCTCCTGGACAGAAACAAAAAAA A CAATCTTTTAAACAGACTGGAGAGT


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




External sources:
dbSNP
no rs
Not found

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


No patient found in CFTR-NGS

20 individuals reported in CFTR-France







Go to CFTRare
VLMCHUUM