Variant #0000717627 (NC_000001.10:g.63885051C>T, NM_013339.3:c.998C>T (ALG6))

Chromosome 1
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.63885051C>T
DNA change (hg38) -
Published as ALG6(NM_013339.3):c.998C>T (p.(Ala333Val)), ALG6(NM_013339.4):c.998C>T (p.A333V)
ISCN -
DB-ID ALG6_000001 See all 13 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) 4.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG6 NM_013339.3 +/. - c.998C>T r.(?) p.(Ala333Val)


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