Variant #0000044888 (NC_000016.9:g.31105879T>C, NM_024006.4:c.172A>G (VKORC1))

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.31105879T>C
DNA change (hg38) g.31094558T>C
Published as -
ISCN -
DB-ID VKORC1_000014 See all 2 reported entries
Variant remarks expression cloning HEK293 cells, 0.21 VKOR activity
Reference PubMed: Rost 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-10-12 22:28:06 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
VKORC1 NM_024006.4 +/. 1 c.172A>G r.(?) p.Arg58Gly -


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