catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.1707T>A
Protein name NP_000483.3:p.(Tyr569*)
Genomic name (hg19) chr7:g.117230434T>A    UCSC    gnomAD
#Exon/intron exon 13
Legacy Name Y569X
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence CAGTATACAAAGATGCTGATTTGTA T TTATTAGACTCTCCTTTTGGATACC
Mutant sequence CAGTATACAAAGATGCTGATTTGTA A TTATTAGACTCTCCTTTTGGATACC


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




External sources:

Not found		dbSNP
no rs
Not found

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


No patient found in CFTR-NGS

1 individual reported in CFTR-France







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