Variant #0001046025 (NC_000005.9:g.176940769G>A, NM_016222.2:c.1015C>T (DDX41))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.176940769G>A
DNA change (hg38) -
Published as DDX41(NM_016222.4):c.1015C>T (p.R339C)
ISCN -
DB-ID DDX41_000032
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX41 NM_016222.2 ?/. - c.1015C>T r.(?) p.(Arg339Cys)
DOK3 NM_024872.2 ?/. - c.-3916C>T r.(?) p.(=)


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