Variant #0000619634 (NC_000023.10:g.48760016C>T, NM_005660.1:c.*699G>A (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.48760016C>T
DNA change (hg38) g.48902739C>T
Published as PQBP1(NM_005710.2):c.585C>T (p.S195=)
ISCN -
DB-ID TIMM17B_000008 See all 2 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) 0.00044 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 -?/. - c.585C>T r.(?) p.(Ser195=)
SLC35A2 NM_005660.1 -?/. - c.*699G>A r.(=) p.(=)
PQBP1 NM_005710.2 -?/. - c.585C>T r.(?) p.(Ser195=)
TIMM17B NM_005834.3 -?/. - c.-4739G>A r.(?) p.(=)


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