Variant #0001033838 (NC_000003.11:g.183960671C>T, NM_005787.5:c.1084G>A (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.183960671C>T
DNA change (hg38) -
Published as ALG3(NM_001006941.2):c.940G>A (p.V314I), ALG3(NM_005787.6):c.1084G>A (p.(Val362Ile))
ISCN -
DB-ID ALG3_000023 See all 2 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) 0.00117 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG3 NM_005787.5 ?/. - c.1084G>A r.(?) p.(Val362Ile)
VWA5B2 NM_138345.1 ?/. - c.*845C>T r.(=) p.(=)


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