Variant #0000675277 (NC_000022.10:g.19163734C>T, NM_005984.3:c.845G>A (SLC25A1))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.19163734C>T
DNA change (hg38) g.19176221C>T
Published as -
ISCN -
DB-ID SLC25A1_000045
Variant remarks overexpression in deficient fibroblasts showed severely impaired CIC activity (below 25%)
Reference PubMed: Edvardson 2013, Journal: Edvardson 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) 1.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A1 NM_005984.3 +/+ 9 c.845G>A r.(?) p.Arg282His


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