Variant #0000557491 (NC_000016.9:g.22144257G>A, NM_001164579.1:c.*52056G>A (C16orf52))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.22144257G>A
DNA change (hg38) g.22132936G>A
Published as VWA3A(NM_173615.4):c.1909G>A (p.G637S)
ISCN -
DB-ID C16orf52_000003
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) 0.00053 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     
C16orf52 NM_001164579.1 -?/. - c.*52056G>A r.(=) p.(=)
VWA3A NM_173615.3 -?/. - c.1909G>A r.(?) p.(Gly637Ser)


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