Variant #0000557944 (NC_000016.9:g.31097770C>T, NM_024006.4:c.*4685G>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.31097770C>T
DNA change (hg38) g.31086449C>T
Published as PRSS53(NM_001039503.2):c.551G>A (p.R184H)
ISCN -
DB-ID PRSS53_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) 0.00037 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 2019-07-18 18:22:55 +02:00 (CEST)
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     

Haplotype     
PRSS53 NM_001039503.2 ?/. - c.551G>A r.(?) p.(Arg184His) -
ZNF646 NM_014699.3 ?/. - c.*3357C>T r.(=) p.(=) -
VKORC1 NM_024006.4 ?/. - c.*4685G>A r.(=) p.(=) -
ZNF668 NM_024706.4 ?/. - c.-12813G>A r.(?) p.(=) -


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