Variant #0000963564 (NC_000005.9:g.176940816C>T, NM_016222.2:c.968G>A (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.176940816C>T
DNA change (hg38) -
Published as DDX41(NM_016222.4):c.968G>A (p.R323H)
ISCN -
DB-ID DDX41_000018 See all 2 reported entries
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) 0 View details
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 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX41 NM_016222.2 +/. - c.968G>A r.(?) p.(Arg323His)
DOK3 NM_024872.2 +/. - c.-3963G>A r.(?) p.(=)


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