catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.2988+1616_3367+356delins62
Protein name NP_000483.3:p.(Leu997Glufs*11)
Genomic name (hg19) chr7:g.117248423_117252218delins62    UCSC    
#Exon/intron intron 18
Legacy Name Del exon 17a-17b
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass CF-causing
WT sequence ACAGGCGCGCACCACCATGCCTGGA TAATTT [3784bp] CATACT CATATTGGTGAAGGGTCCTAGCTTC
Mutant sequence ACAGGCGCGCACCACCATGCCTGGA 62-------------------- CATATTGGTGAAGGGTCCTAGCTTC


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





External sources:

Not found
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

2 individuals reported in CFTR-France







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