Variant #0001006796 (NC_000023.10:g.48759674A>G, NM_005660.1:c.*1041T>C (SLC35A2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48759674A>G
DNA change (hg38) -
Published as PQBP1(NM_001032382.1):c.457A>G (p.(Arg153Gly))
ISCN -
DB-ID TIMM17B_000032
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 -?/. - c.457A>G r.(?) p.(Arg153Gly)
SLC35A2 NM_005660.1 -?/. - c.*1041T>C r.(=) p.(=)
PQBP1 NM_005710.2 -?/. - c.457A>G r.(?) p.(Arg153Gly)
TIMM17B NM_005834.3 -?/. - c.-4397T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.