Variant #0000299541 (NC_000023.10:g.48762368C>T, NM_005660.1:c.818G>A (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.48762368C>T
DNA change (hg38) g.48905091C>T
Published as SLC35A2(NM_001042498.3):c.818G>A (p.G273D)
ISCN -
DB-ID SLC35A2_000013 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_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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 +/. - c.*2007C>T r.(=) p.(=)
SLC35A2 NM_005660.1 +/. - c.818G>A r.(?) p.(Gly273Asp)
PQBP1 NM_005710.2 +/. - c.*2007C>T r.(=) p.(=)
TIMM17B NM_005834.3 +/. - c.-7091G>A r.(?) p.(=)


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