catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3410T>G
Protein name NP_000483.3:p.(Met1137Arg)
Genomic name (hg19) chr7:g.117254709T>G    UCSC    gnomAD
#Exon/intron exon 21
Legacy Name M1137R
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence GTTGGTATTATCCTGACTTTAGCCA T GAATATCATGAGTACATTGCAGTGG
Mutant sequence GTTGGTATTATCCTGACTTTAGCCA G GAATATCATGAGTACATTGCAGTGG


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
C65 2e-05 0 0.998
VUS5 VUS5 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







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