Variant #0000867415 (NC_000023.10:g.48762196G>A, NM_005660.1:c.990C>T (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.48762196G>A
DNA change (hg38) -
Published as SLC35A2(NM_001282651.1):c.1074C>T (p.L358=), SLC35A2(NM_005660.3):c.990C>T (p.(Leu330=))
ISCN -
DB-ID TIMM17B_000026 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) 0.00056 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 -?/. - c.*1835G>A r.(=) p.(=)
SLC35A2 NM_005660.1 -?/. - c.990C>T r.(?) p.(Leu330=)
PQBP1 NM_005710.2 -?/. - c.*1835G>A r.(=) p.(=)
TIMM17B NM_005834.3 -?/. - c.-6919C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.