Variant #0001006794 (NC_000023.10:g.48759551_48759571del, NM_005660.1:c.*1161_*1181del (SLC35A2))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48759551_48759571del
DNA change (hg38) -
Published as PQBP1(NM_005710.2):c.334_354delAGGGGCCATGACAAGTCGGAC (p.G113_R119del)
ISCN -
DB-ID PQBP1_000017 See all 3 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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.334_354del r.(?) p.(Gly113_Arg119del)
SLC35A2 NM_005660.1 -/. - c.*1161_*1181del r.(=) p.(=)
PQBP1 NM_005710.2 -/. - c.334_354del r.(?) p.(Gly113_Arg119del)
TIMM17B NM_005834.3 -/. - c.-4277_-4257del r.(?) p.(=)


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