catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3468G>A
Protein name NP_000483.3:p.(=)
Genomic name (hg19) chr7:g.117254767G>A    UCSC    gnomAD
#Exon/intron exon 21
Legacy Name L1156L (3600G/A)
Type in CFTR-NGS catalogue -
Class in CFTR-France disease-causing
Subclass varying clinical consequence
WT sequence ACTCCAGCATAGATGTGGATAGCTT G GTAAGTCTTATCATCTTTTTAACTT
Mutant sequence ACTCCAGCATAGATGTGGATAGCTT A GTAAGTCTTATCATCTTTTTAACTT


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

5 individuals reported in CFTR-France







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