Variant #0000576275 (NC_000023.10:g.48759558A>G, NM_005660.1:c.*1157T>C (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.48759558A>G
DNA change (hg38) g.48902281A>G
Published as PQBP1(NM_005710.2):c.341A>G (p.H114R)
ISCN -
DB-ID TIMM17B_000006
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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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.341A>G r.(?) p.(His114Arg)
SLC35A2 NM_005660.1 -?/. - c.*1157T>C r.(=) p.(=)
PQBP1 NM_005710.2 -?/. - c.341A>G r.(?) p.(His114Arg)
TIMM17B NM_005834.3 -?/. - c.-4281T>C r.(?) p.(=)


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