Variant NM_000492.4:c.2374C>T


Variant details:
Name NM_000492.4:c.2374C>T
Protein name NP_000483.3:p.(Arg792*)
Genomic name (hg19) chr7:g.117232595C>T    UCSC    
#Exon/intron exon 14
Legacy Name R792X
Class disease-causing
Subclass CF-causing
WT sequence TCACCGAAAGACAACAGCATCCACA C GAAAAGTGTCACTGGCCCCTCAGGC
Mutant sequence TCACCGAAAGACAACAGCATCCACA T GAAAAGTGTCACTGGCCCCTCAGGC

Other databases:
dbSNP
rs145449046







Pathogenicity predictors:

Not found





No patient found in CFTR-NGS catalogue


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

TOTAL NUMBER OF PATIENTS 11
CF 10
Fetal bowel anomalies 1




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

Detailed genotypes:
Phenotype Patient ID Variant status Additional variants
CF 4718heterozygotevarying clinical consequence - Trans
CF 3154heterozygoteCF-causing - Trans
CF 2201heterozygoteCF-causing- Undef
CF 2007heterozygoteCF-causing- Undef
CF 1590heterozygoteCF-causing- Undef
CF 896heterozygoteCF-causing - Trans
CF 341heterozygoteCF-causing- Undef
CF 261heterozygoteCF-causing- Undef
CF 175heterozygoteCF-causing- Undef
CF 4610heterozygoteCF-causing - Trans
Fetal bowel anomalies 916heterozygoteCF-causing - Trans


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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