Variant #0000913709 (NC_000011.9:g.77825024G>A, NM_024079.4:c.685C>T (ALG8))

Chromosome 11
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.77825024G>A
DNA change (hg38) -
Published as ALG8(NM_001007027.2):c.685C>T (p.R229*), ALG8(NM_024079.5):c.685C>T (p.R229*)
ISCN -
DB-ID ALG8_000034 See all 3 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) 2.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG8 NM_024079.4 +/. - c.685C>T r.(?) p.(Arg229*)


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