Variant #0000275083 (NC_000008.10:g.42233230G>A, NM_014420.2:c.230C>T (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.42233230G>A
DNA change (hg38) g.42375712G>A
Published as DKK4(NM_014420.3):c.230C>T (p.A77V)
ISCN -
DB-ID DKK4_000001
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLB NM_002690.2 ?/. - c.*4055G>A r.(=) p.(=)
DKK4 NM_014420.2 ?/. - c.230C>T r.(?) p.(Ala77Val)


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