catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117303563T/TA


CFTR-NGS Variant details:
Name NM_000492.4:c.3964-1161dupA
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117303581dup    UCSC    
#Exon/intron intron 24
Type in CFTR-NGS catalogue repeat
Class in CFTR-France not reported
WT sequence TCCAGCTAAAAAAAAAAAAAAAAAA - CAAGCCATTGGTCCTAACACAACTT
Mutant sequence TCCAGCTAAAAAAAAAAAAAAAAAA A CAAGCCATTGGTCCTAACACAACTT


Additional information:
MAF (GnomAD) 8.63e-03
Splicing prediction (SpliceAI) AG: 0.00 (-1)
AL: 0.00 (23)
DG: 0.00 (-34)
DL: 0.00 (-30)




External sources:

Not found

Not found
dbSNP
no rs

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


4 individuals (out of 136) carrying this variant are reported in CFTR-NGS catalogue:

TOTAL NUMBER OF INDIVIDUALS 4
CF 3
CFTR-RD1
  • CFTR-RD  1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
21CFMontpellier150517_varilhheterozygous PASS 1226 466
22CFMontpellier150517_varilhheterozygous PASS 1673 422
9879CFMontpellier160218_varilhheterozygous PASS 1028 328
6008CFTR-RDMontpellier160218_varilhheterozygous PASS 967 317





Go to CFTRare
VLMCHUUM