Variant #0001002968 (NC_000017.10:g.1631346_1631347del, NM_001163809.1:c.3093_3094del (WDR81))

Chromosome 17
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.1631346_1631347del
DNA change (hg38) -
Published as WDR81(NM_001163809.1):c.3093_3094delGG (p.(Glu1032fs))
ISCN -
DB-ID WDR81_000132
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
WDR81 NM_001163809.1 ?/. - c.3093_3094del r.(?) p.(Glu1032Glyfs*46)


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