Variant #0001054678 (NC_000013.10:g.52593047A>G, NC_000013.10(NM_001004127.2):c.45-2A>G (ALG11))

Chromosome 13
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.52593047A>G
DNA change (hg38) -
Published as ALG11(NM_001004127.3):c.45-2A>G
ISCN -
DB-ID ALG11_000022
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG11 NM_001004127.2 ?/. - c.45-2A>G r.spl? p.?
UTP14C NM_021645.5 ?/. - c.-6513A>G r.(?) p.(=)


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