Variant #0000984719 (NC_000023.10:g.48772479C>T, NM_005660.1:c.-3566G>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.48772479C>T
DNA change (hg38) -
Published as PIM2(NM_006875.4):c.413G>A (p.(Gly138Asp))
ISCN -
DB-ID SLC35A2_000069
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) 0.00055 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
SLC35A2 NM_005660.1 -?/. - c.-3566G>A r.(?) p.(=)
PIM2 NM_006875.3 -?/. - c.413G>A r.(?) p.(Gly138Asp)


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