Variant NM_000492.4:c.137C>T


Variant details:
Name NM_000492.4:c.137C>T
Protein name NP_000483.3:p.(Ala46Val)
Genomic name (hg19) chr7:g.117144390C>T    UCSC    gnomAD
#Exon/intron exon 2
Legacy Name A46V
Class VUS
Subclass VUS3
WT sequence TACCAAATCCCTTCTGTTGATTCTG C TGACAATCTATCTGAAAAATTGGAA
Mutant sequence TACCAAATCCCTTCTGTTGATTCTG T TGACAATCTATCTGAAAAATTGGAA


External sources:

Not found		dbSNP
rs151020603






Pathogenicity predictions:
AGVGD MAPP SIFT PPH2
C0 0.0119 0.47 1
VUS1 VUS4 VUS1 VUS5

Color code:   non disease-causing <   VUS1 <   VUS2 <   VUS3 <   VUS4 <   VUS5 <   disease-causing



No patient found in CFTR-NGS catalogue

No patient found in CFTR-France



            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.