catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.859A>T
Protein name NP_000483.3:p.(Asn287Tyr)
Genomic name (hg19) chr7:g.117176717A>T    UCSC    gnomAD
#Exon/intron exon 7
Legacy Name N287Y
Type in CFTR-NGS catalogue -
Class in CFTR-France VUS
Subclass VUS3
WT sequence AGAAGCAATGGAAAAAATGATTGAA A ACTTAAGACAGTAAGTTGTTCCAAT
Mutant sequence AGAAGCAATGGAAAAAATGATTGAA T ACTTAAGACAGTAAGTTGTTCCAAT


Additional information:
MAF (GnomAD) -
Splicing prediction (SpliceAI) -

External sources:

Not found
dbSNP
no rs

Variant validation:
Sanger
(present/not present/not verified)
Minigene
(effect/no effect/not performed)
present not performed


Pathogenicity predictions:
AGVGD MAPP SIFT PPH2
C15 0.03795 0.05 0.744
VUS1 VUS4 VUS4 VUS4
Color code:   non disease-causing <   VUS1 <   VUS2 <   VUS3 <   VUS4 <   VUS5 <   disease-causing


No patient found in CFTR-NGS

1 individual reported in CFTR-France







Go to CFTRare
VLMCHUUM