Variant #0000990878 (NC_000001.10:g.224621627G>A, NM_025160.6:c.181C>T (WDR26))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.224621627G>A
DNA change (hg38) -
Published as WDR26(NM_025160.6):c.181C>T (p.(Pro61Ser))
ISCN -
DB-ID CNIH3_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
WDR26 NM_025160.6 -?/. - c.181C>T r.(?) p.(Pro61Ser)
CNIH3 NM_152495.1 -?/. - c.-183250G>A r.(?) p.(=)


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