Variant #0000725652 (NC_000016.9:g.22132379T>A, NM_001164579.1:c.*40178T>A (C16orf52))

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.22132379T>A
DNA change (hg38) -
Published as VWA3A(NM_173615.4):c.1207T>A (p.L403M)
ISCN -
DB-ID C16orf52_000006
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
C16orf52 NM_001164579.1 ?/. - c.*40178T>A r.(=) p.(=)
VWA3A NM_173615.3 ?/. - c.1207T>A r.(?) p.(Leu403Met)


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