catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3475T>C
Protein name NP_000483.3:p.(Ser1159Pro)
Genomic name (hg19) chr7:g.117267582T>C    UCSC    gnomAD
#Exon/intron exon 22
Legacy Name S1159P
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
WT sequence GTTGTTATTTTTATTTCAGATGCGA T CTGTGAGCCGAGTCTTTAAGTTCAT
Mutant sequence GTTGTTATTTTTATTTCAGATGCGA C CTGTGAGCCGAGTCTTTAAGTTCAT


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

External sources:
dbSNP
no rs

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


Pathogenicity predictions:
AGVGD MAPP SIFT PPH2
0.01 0.973
no class no class VUS5 VUS5
Color code:   non disease-causing <   VUS1 <   VUS2 <   VUS3 <   VUS4 <   VUS5 <   disease-causing


No patient found in CFTR-NGS

No patient found in CFTR-France







Go to CFTRare
VLMCHUUM