Variant #0000929591 (NC_000009.11:g.32492446del, NM_014314.3:c.516del (DDX58))

Chromosome 9
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.32492446del
DNA change (hg38) -
Published as DDX58(NM_014314.3):c.516delA (p.K172Nfs*17), DDX58(NM_014314.4):c.516delA (p.K172Nfs*17)
ISCN -
DB-ID DDX58_000025 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) 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX58 NM_014314.3 ?/. - c.516del r.(?) p.(Lys172AsnfsTer17)


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