Variant #0001046867 (NC_000023.10:g.48759525_48759566del, NM_005660.1:c.*1153_*1194del (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.48759525_48759566del
DNA change (hg38) -
Published as PQBP1(NM_005710.2):c.308_349del (p.L103_K116del)
ISCN -
DB-ID TIMM17B_000035
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 2025-07-08 13:22:38 +02:00 (CEST)
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.308_349del r.(?) p.(Leu103_Lys116del)
SLC35A2 NM_005660.1 ?/. - c.*1153_*1194del r.(=) p.(=)
PQBP1 NM_005710.2 ?/. - c.308_349del r.(?) p.(Leu103_Lys116del)
TIMM17B NM_005834.3 ?/. - c.-4285_-4244del r.(?) p.(=)


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