Variant #0001027508 (NC_000023.10:g.48760007A>G, NM_005660.1:c.*708T>C (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.48760007A>G
DNA change (hg38) -
Published as PQBP1(NM_005710.2):c.578-2A>G
ISCN -
DB-ID TIMM17B_000033
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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 ?/. - c.578-2A>G r.spl? p.?
SLC35A2 NM_005660.1 ?/. - c.*708T>C r.(=) p.(=)
PQBP1 NM_005710.2 ?/. - c.578-2A>G r.spl? p.?
TIMM17B NM_005834.3 ?/. - c.-4730T>C r.(?) p.(=)


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