Variant #0000679836 (NC_000013.10:g.52598272C>T, NM_001004127.2:c.406C>T (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.52598272C>T
DNA change (hg38) -
Published as ALG11(NM_001004127.2):c.406C>T (p.R136C, p.(Arg136Cys))
ISCN -
DB-ID ALG11_000016 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) 0.00024 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG11 NM_001004127.2 ?/. - c.406C>T r.(?) p.(Arg136Cys)
UTP14C NM_021645.5 ?/. - c.-1288C>T r.(?) p.(=)


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