Variant #0000679837 (NC_000013.10:g.52598753del, NM_001004127.2:c.887del (ALG11))

Chromosome 13
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.52598753del
DNA change (hg38) -
Published as ALG11(NM_001004127.2):c.887delA (p.K296Rfs*2)
ISCN -
DB-ID ALG11_000017
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_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 2020-09-15 15:50:26 +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.887del r.(?) p.(Lys296ArgfsTer2)
UTP14C NM_021645.5 +?/. - c.-807del r.(?) p.(=)


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