catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.331C>G
Protein name NP_000483.3:p.(Pro111Ala)
Genomic name (hg19) chr7:g.117171010C>G    UCSC    gnomAD
#Exon/intron exon 4
Legacy Name P111A
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CFTR-RD-causing
WT sequence GGGAAGAATCATAGCTTCCTATGAC C CGGATAACAAGGAGGAACGCTCTAT
Mutant sequence GGGAAGAATCATAGCTTCCTATGAC G CGGATAACAAGGAGGAACGCTCTAT


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)
presentnot performed


Pathogenicity predictions:
AGVGD MAPP SIFT PPH2
C0 0.665 0.76 0.087
VUS1 VUS1 VUS1 VUS1
Color code:   non disease-causing <   VUS1 <   VUS2 <   VUS3 <   VUS4 <   VUS5 <   disease-causing


No patient found in CFTR-NGS

No patient found in CFTR-France







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