catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117229957C/T


CFTR-NGS Variant details:
Name NM_000492.4:c.1680-450C>T
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117229957C>T    UCSC    gnomAD
#Exon/intron intron 12
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence TCTTTTTGGTGTCCTCACCAAAACC C AACATCTTCAAGGGCAGGAACTGTA
Mutant sequence TCTTTTTGGTGTCCTCACCAAAACC T AACATCTTCAAGGGCAGGAACTGTA


Additional information:
MAF (GnomAD) 5.17e-04
Splicing prediction (SpliceAI) AG: 0.00 (3)
AL: 0.00 (-42)
DG: 0.00 (-2)
DL: 0.00 (22)




External sources:

Not found
Not found		dbSNP
rs946514719
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
CFTR-RD1
  • CFTR-RD  1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
17MU00956CFTR-RDCochin150419_Altieriheterozygous PASS 3429 312





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