catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117160263T/C


CFTR-NGS Variant details:
Name NM_000492.4:c.274-10690T>C
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117160263T>C    UCSC    gnomAD
#Exon/intron intron 3
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence TGTTGTATTTGTCTCTTTCTTGATA T ATGAGAGAATATTTTCCCTAGCCTG
Mutant sequence TGTTGTATTTGTCTCTTTCTTGATA C ATGAGAGAATATTTTCCCTAGCCTG


Additional information:
MAF (GnomAD) 1.47e-04
Splicing prediction (SpliceAI) AG: 0.00 (8)
AL: 0.00 (22)
DG: 0.00 (36)
DL: 0.00 (-40)




External sources:

Not found
Not found		dbSNP
rs568902225
Not found

Variant validation:
Sanger
(present/not present/not verified)
 Minigene
(effect/no effect/not performed)
not verifiednot performed



No patient found in CFTR-France


1 individual (out of 136) carrying this variant is reported in CFTR-NGS catalogue:

TOTAL NUMBER OF INDIVIDUALS 1
Asymptomatic 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
MUCO07319AsymptomaticMontpellier100714_varilhheterozygous PASS 2875 223





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