Variant #0000717210 (NC_000001.10:g.224621462T>A, NM_025160.6:c.346A>T (WDR26))

Chromosome 1
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.224621462T>A
DNA change (hg38) -
Published as WDR26(NM_001115113.3):c.346A>T (p.K116*)
ISCN -
DB-ID CNIH3_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR26 NM_025160.6 +/. - c.346A>T r.(?) p.(Lys116Ter)
CNIH3 NM_152495.1 +/. - c.-183415T>A r.(?) p.(=)


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