Variant #0001033839 (NC_000003.11:g.183963586A>G, NM_005787.5:c.211T>C (ALG3))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.183963586A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALG3_000001 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG3 NM_005787.5 +?/. - c.211T>C r.(?) p.(Trp71Arg)
ECE2 NM_014693.3 +?/. - c.-3897A>G r.(?) p.(=)
CAMK2N2 NM_033259.2 +?/. - c.*14359T>C r.(=) p.(=)
VWA5B2 NM_138345.1 +?/. - c.*3760A>G r.(=) p.(=)


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