Variant #0001036975 (NC_000008.10:g.42231799A>G, NM_014420.2:c.494T>C (DKK4))

Chromosome 8
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.42231799A>G
DNA change (hg38) -
Published as DKK4(NM_014420.3):c.494T>C (p.(Ile165Thr))
ISCN -
DB-ID DKK4_000004
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) 0.00074 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 2025-05-05 21:14:00 +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     
POLB NM_002690.2 ?/. - c.*2624A>G r.(=) p.(=)
DKK4 NM_014420.2 ?/. - c.494T>C r.(?) p.(Ile165Thr)


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