Variant #0000876499 (NC_000011.9:g.45832509A>G, NM_018389.4:c.718A>G (SLC35C1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45832509A>G
DNA change (hg38) g.45810958A>G
Published as -
ISCN -
DB-ID SLC35C1_000031
Variant remarks corrected after consultation authors
Reference PubMed: van de Vijver 2012, Journal: van de Vijver 2012
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.09173 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-08-15 17:50:58 +02:00 (CEST)
Date last edited 2022-09-27 17:44:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35C1 NM_018389.4 -/. - c.718A>G r.(?) p.(Ile240Val)


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