Variant #0000688039 (NC_000001.10:g.224619194C>T, NM_025160.6:c.612G>A (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.224619194C>T
DNA change (hg38) -
Published as WDR26(NM_025160.7):c.612G>A (p.L204=)
ISCN -
DB-ID CNIH3_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR26 NM_025160.6 -?/. - c.612G>A r.(?) p.(Leu204=)
CNIH3 NM_152495.1 -?/. - c.-185683C>T r.(?) p.(=)


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