Variant #0000299540 (NC_000023.10:g.48767241del, NM_005660.1:c.124del (SLC35A2))

Chromosome X
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.48767241del
DNA change (hg38) g.48909964del
Published as SLC35A2(NM_001282651.2):c.208delG (p.V70Cfs*53)
ISCN -
DB-ID SLC35A2_000019
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-19 21:20:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35A2 NM_005660.1 +/. - c.124del r.(?) p.(Val42CysfsTer53)
PIM2 NM_006875.3 +/. - c.*4167del r.(?) p.(=)


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