Variant #0000948534 (NC_000005.9:g.176942946_176942949dup, NM_016222.2:c.415_418dup (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.176942946_176942949dup
DNA change (hg38) -
Published as DDX41(NM_016222.4):c.415_418dupGATG (p.D140Gfs*2)
ISCN -
DB-ID DDX41_000005 See all 4 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM193B NM_001190946.1 +/. - c.*4235_*4238dup r.(=) p.(=)
DDX41 NM_016222.2 +/. - c.415_418dup r.(?) p.(Asp140Glyfs*2)


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