Variant #0000679617 (NC_000012.11:g.6127833T>C, NM_000552.3:c.4751A>G (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.6127833T>C
DNA change (hg38) -
Published as VWF(NM_000552.3):c.4751A>G (p.Y1584C, p.(Tyr1584Cys)), VWF(NM_000552.4):c.4751A>G (p.Y1584C), VWF(NM_000552.5):c.4751A>G (p.Y1584C)
ISCN -
DB-ID VWF_000117 See all 22 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) 0.00271 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.4751A>G r.(?) p.(Tyr1584Cys)


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