Variant #0000659344 (NC_000023.10:g.48760636A>G, NM_005660.1:c.*79T>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.48760636A>G
DNA change (hg38) g.48903359A>G
Published as SLC35A2(NM_005660.3):c.*79T>C
ISCN -
DB-ID TIMM17B_000016
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 2020-03-23 16:13:27 +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.*275A>G r.(=) p.(=)
SLC35A2 NM_005660.1 -?/. - c.*79T>C r.(=) p.(=)
PQBP1 NM_005710.2 -?/. - c.*275A>G r.(=) p.(=)
TIMM17B NM_005834.3 -?/. - c.-5359T>C r.(?) p.(=)


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