Variant #0000169017 (NC_000023.10:g.41200777dup, DDX3X(NM_001356.3):c.192dup)

Individual ID 00103879
Chromosome X
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41200777dup
DNA change (hg38) g.41341524dup
Published as -
ISCN -
DB-ID DDX3X_000008
Variant remarks -
Reference PubMed: Eldomery 2017, Journal: Eldomery 2017
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX3X NM_001356.3 +/. 4 c.192dup r.(?) p.(Asp65Argfs*2)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000104337 DNA SEQ;SEQ-NG - - DDX3X 1 Johan den Dunnen