Variant #0000329725 (NC_000003.11:g.183957251T>A, NM_005787.5:c.*3051A>T (ALG3))

Chromosome 3
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.183957251T>A
DNA change (hg38) g.184239463T>A
Published as VWA5B2(NM_138345.1):c.2272T>A (p.(Ser758Thr))
ISCN -
DB-ID VWA5B2_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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ALG3 NM_005787.5 ?/. - c.*3051A>T r.(=) p.(=)
VWA5B2 NM_138345.1 ?/. - c.2272T>A r.(?) p.(Ser758Thr)


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