Variant NM_000492.4:c.532G>A


Variant details:
Name NM_000492.4:c.532G>A
Protein name NP_000483.3:p.(Gly178Arg)
Genomic name (hg19) chr7:g.117174372G>A    UCSC    
#Exon/intron exon 5
Legacy Name G178R
Class disease-causing
Subclass CF-causing
WT sequence CCGTGTTCTAGATAAAATAAGTATT G GACAACTTGTTAGTCTCCTTTCCAA
Mutant sequence CCGTGTTCTAGATAAAATAAGTATT A GACAACTTGTTAGTCTCCTTTCCAA

Other databases:
dbSNP
rs80282562



Pathogenicity predictors:

Functional studies:


Reference PMID Splicing mRNA level Maturation Localization Channel fonction (Cl-) Bicarbonate
Seibert et al, 1997 9305991 ✓ ✓ ✓
Yu et al, 2012 22293084 ✓ ✓ ✓
Raynal et al, 2013 23381846 ✓
Sosnay et al, 2013 23974870 ✓ ✓


« ✓ » indicates the type of analysis performed and not the results


Response to modulators:


Modulator FDA approval EMA approval in vitro / ex vivo data clinical data
IVA yes yesno yes
TEZ-IVA yesnoyesno
ELX-TEZ-IVA yesnoyesno


clinical and functional data are provided by Vertex


No patient found in CFTR-NGS catalogue


10 patients carrying this variant are reported in CFTR-France:

TOTAL NUMBER OF PATIENTS 10
CF 10




Color code:   non disease-causing <   likely benign <   VUS <   likely pathogenic <   disease-causing

Detailed genotypes:
Phenotype Patient ID Variant status Additional variants
CF 122heterozygoteCF-causing - Trans
CF 2600heterozygoteCF-causing- Undef
CF 1298heterozygoteCF-causing - Trans
CF 681heterozygoteCF-causing - Trans
CF 336heterozygoteCF-causing - Trans
CF 334heterozygoteCF-causing - Trans
CF 283heterozygoteCF-causing- Undef
CF 167heterozygoteCF-causing- Undef
CF 160heterozygoteCF-causing - Trans
CF 6093heterozygoteCF-causing- Undef


Color code:   non disease-causing <   likely benign <   VUS <   likely pathogenic <   disease-causing



            CFTR variants are clustered into five groups:
  • CF-causing: when in trans with another CF-causing mutation, will result in CF.
  • CFTR-RD causing: when in trans with a CF-causing mutation, will result in CFTR-related disorders (CFTR-RD) such as chronic pancreatitis, bronchiectasis, CRS-NP (chronic rhinosinusitis with or without nasal polyposis) or CBAVD (congenital absence of vas deferens), according to Bombieri C et al., 2011.
  • Varying clinical consequence: when in trans with another CF-causing mutation, can either result in CF or in a CFTR-RD.
  • Non disease-causing: when in trans with a CF-causing mutation, will not cause CF, nor CFTR-RD.
  • VUS (Variant of unknown clinical significance): unclassified because of insufficient data.



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