Variant NM_000492.4:c.1163C>T


Variant details:
Name NM_000492.4:c.1163C>T
Protein name NP_000483.3:p.(Thr388Met)
Genomic name (hg19) chr7:g.117182116C>T    UCSC    
#Exon/intron exon 9
Legacy Name T388M
Class VUS
WT sequence TATAAGACATTGGAATATAACTTAA C GACTACAGAAGTAGTGATGGAGAAT
Mutant sequence TATAAGACATTGGAATATAACTTAA T GACTACAGAAGTAGTGATGGAGAAT

Other databases:

Not found		dbSNP
rs143860237



Pathogenicity predictors:





No patient found in CFTR-NGS catalogue


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

TOTAL NUMBER OF PATIENTS 1
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
Other 4760heterozygote


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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