catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.[3469-331_3469-295del;3469-189_3717+3822del]
Protein name NP_000483.3:p.?
Genomic name (hg19) chr7:g.[117267245_117267281del; 117267387_117271646del]    UCSC    
#Exon/intron intron 21
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence CATTTTATTATAATATACCGGTTAT ACAGCA [25bp] ATAAAT TTTCTCTTTGATGTCATCTATTCCC ; CAGAGCCCATTTATATAAGTCCTGG TTATTT [4248bp] AACTGG AACTTTTTGGAGAGCCTCCAGGCTG
Mutant sequence CATTTTATTATAATATACCGGTTAT -------------------- TTTCTCTTTGATGTCATCTATTCCC ; CAGAGCCCATTTATATAAGTCCTGG ---------------------- AACTTTTTGGAGAGCCTCCAGGCTG


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





External sources:

Not found		dbSNP
no rs
Not found
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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