Variant #0000675269 (NC_000022.10:g.19163689T>C, NM_005984.3:c.890A>G (SLC25A1))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.19163689T>C
DNA change (hg38) g.19176176T>C
Published as -
ISCN -
DB-ID SLC25A1_000046
Variant remarks overexpression in deficient fibroblasts showed reduced CIC activity: see discussion in article
Reference PubMed: Nota 2013, Journal: Nota 2013, PubMed: Pop 2018, Journal: Pop 2018
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Eric Wever
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-08-05 14:33:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A1 NM_005984.3 +?/+? 9 c.890A>G r.(?) p.Tyr297Cys


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