Variant NM_000492.4:c.1007T>A


Variant details:
Name NM_000492.4:c.1007T>A
Protein name NP_000483.3:p.(Ile336Lys)
Genomic name (hg19)     chr7:g.117180291T>A    UCSC    
Genomic name (hg38) chr7:g.117540237T>A    UCSC
#Exon/intron exon 8
Legacy Name I336K
Class disease-causing
Subclass CF-causing
WT sequence ATCAAAGGAATCATCCTCCGGAAAA T ATTCACCACCATCTCATTCTGCATT
Mutant sequence ATCAAAGGAATCATCCTCCGGAAAA A ATTCACCACCATCTCATTCTGCATT

Other databases:
dbSNP
rs397508139



Pathogenicity predictors:

Functional studies:


Reference PMID Splicing mRNA level Maturation Localization Channel fonction (Cl-) Bicarbonate
Van Goor et al, 2014 23891399 ✓ ✓ ✓
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
IVAnononono
TEZ-IVA yesnoyesno
ELX-TEZ-IVA yesnoyesno
VNZ-TEZ-DIVA yesnono yes

clinical and functional data presented above are provided by Vertex


No patient found in CFTR-NGS catalogue


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

TOTAL NUMBER OF PATIENTS 6
CF 5
CFTR-RD1
  • Other  1




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

Detailed genotypes:
Phenotype Patient ID Variant status Additional variants
CF 276heterozygoteCF-causing - Trans
CF 6248heterozygoteCF-causing- Undef
CF 3057heterozygoteCF-causing - Trans
CF 6171heterozygoteCF-causing- Undef
CF 6166heterozygoteCF-causing- Undef
Other 3058heterozygoteCF-causing - Trans


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



            CFTR variants are clustered into five groups (click here for more details about the classification of variants):
  • 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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