Variant #0000454337 (NC_000016.9:g.31104878G>C, NC_000016.9(NM_024006.4):c.174-136C>G (VKORC1))

Chromosome 16
Allele Both (homozygous)
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.31104878G>C
DNA change (hg38) g.31093557G>C
Published as -
ISCN -
DB-ID VKORC1_000017
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs9934438
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Hye Sun Gwak
Database submission license No license selected
Created by Hye Sun Gwak
Date created 2019-01-28 09:38:06 +01:00 (CET)
Date last edited 2023-01-31 09:41:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
VKORC1 NM_024006.4 ?/. - c.174-136C>G r.(?) p.(?) -



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