Variant #0000725751 (NC_000016.9:g.31104720C>T, NM_024006.4:c.196G>A (VKORC1))

Chromosome 16
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.31104720C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PRSS53_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) 0.0002 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PRSS53 NM_001039503.2 ?/. - c.-4590G>A r.(?) p.(=) -
ZNF646 NM_014699.3 ?/. - c.*10307C>T r.(=) p.(=) -
VKORC1 NM_024006.4 ?/. - c.196G>A r.(?) p.(Val66Met) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.