Variant #0000963563 (NC_000005.9:g.176939360_176939361del, NM_016222.2:c.1586_1587del (DDX41))

Chromosome 5
Allele Unknown
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.176939360_176939361del
DNA change (hg38) -
Published as -
ISCN -
DB-ID DDX41_000017
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX41 NM_016222.2 +/. - c.1586_1587del r.(?) p.(Thr529Argfs*12)
DOK3 NM_024872.2 +/. - c.-2505_-2504del r.(?) p.(=)


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