catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3528del
Protein name NP_000483.3:p.(Lys1177Serfs*15)
Genomic name (hg19) chr7:g.117267635del    UCSC    
#Exon/intron exon 22
Legacy Name 3659delC
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence ACATGCCAACAGAAGGTAAACCTAC C AAGTCAACCAAACCATACAAGAATG
Mutant sequence ACATGCCAACAGAAGGTAAACCTAC - AAGTCAACCAAACCATACAAGAATG


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




External sources:
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

29 individuals reported in CFTR-France







Go to CFTRare
VLMCHUUM