Variant #0000343427 (NC_000012.11:g.6143978C>T, NM_000552.3:c.2561G>A (VWF))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6143978C>T
DNA change (hg38) g.6034812C>T
Published as VWF(NM_000552.3):c.2561G>A (p.R854Q), VWF(NM_000552.5):c.2561G>A (p.R854Q)
ISCN -
DB-ID VWF_000054 See all 56 reported entries
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) 0.00339 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VWF NM_000552.3 +/. - c.2561G>A r.(?) p.(Arg854Gln)


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