Variant #0000999505 (NC_000011.9:g.77832110C>T, NC_000011.9(NM_024079.4):c.478+1G>A (ALG8))

Chromosome 11
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.77832110C>T
DNA change (hg38) -
Published as ALG8(NM_001007027.2):c.478+1G>A, ALG8(NM_024079.4):c.478+1G>A (p.?)
ISCN -
DB-ID ALG8_000045 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) 0.00016 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 2024-08-28 13:16:32 +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     
ALG8 NM_024079.4 ?/. - c.478+1G>A r.spl? p.?


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