catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.3897A>G
Protein name NP_000483.3:p.(=)
Genomic name (hg19) chr7:g.117292919A>G    UCSC    gnomAD
#Exon/intron exon 24
Legacy Name T1299T (4029A/G)
Type in CFTR-NGS catalogue -
Class in CFTR-France non disease-causing
WT sequence AGAAAGTATTTATTTTTTCTGGAAC A TTTAGAAAAAACTTGGATCCCTATG
Mutant sequence AGAAAGTATTTATTTTTTCTGGAAC G TTTAGAAAAAACTTGGATCCCTATG


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

12 individuals reported in CFTR-France







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