catalog




CFTR-NGS variants catalogue


Variant hg19:chr7:117184283TCTGGG/T


CFTR-NGS Variant details:
Name NM_000492.4:c.1209+2122_1209+2126del5
Protein name NP_000483.3:p.(?)
Genomic name (hg19) chr7:g.117184284_117184288del    UCSC    
#Exon/intron intron 9
Type in CFTR-NGS catalogue -
Class in CFTR-France not reported
WT sequence TCAGTTTTGGAGAAGGAAGTGCTAT CTGGG TAACAGTAGTGCTATCTGTTGACTC
Mutant sequence TCAGTTTTGGAGAAGGAAGTGCTAT ----- TAACAGTAGTGCTATCTGTTGACTC


Additional information:
MAF (GnomAD) 1.43e-03
Splicing prediction (SpliceAI) -




External sources:

Not found
Not found		dbSNP
rs1456996808
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
Suspicion of CF 1



Details of NGS patients:
ID Phenotype Laboratory Experiment Variant status Variant filter Quality score Depth of coverage
m9196Suspicion of CFMontpellier150419_Altieriheterozygous LowVariantFreq 639 116





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