Variant #0001014115 (NC_000005.9:g.176942182C>A, NC_000005.9(NM_016222.2):c.644+5G>T (DDX41))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.176942182C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID DDX41_000022
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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM193B NM_001190946.1 +?/. - c.*5002G>T r.(=) p.(=)
DDX41 NM_016222.2 +?/. - c.644+5G>T r.spl? p.?
DOK3 NM_024872.2 +?/. - c.-5329G>T r.(?) p.(=)


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