Variant #0001067676 (NC_000023.10:g.48760071C>T, NM_005660.1:c.*644G>A (SLC35A2))

Chromosome X
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.48760071C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TIMM17B_000036
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
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.640C>T r.(?) p.(Arg214Trp)
SLC35A2 NM_005660.1 ?/. - c.*644G>A r.(=) p.(=)
PQBP1 NM_005710.2 ?/. - c.640C>T r.(?) p.(Arg214Trp)
TIMM17B NM_005834.3 ?/. - c.-4794G>A r.(?) p.(=)


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