Variant #0000839748 (NC_000010.10:g.50954002G>A, NM_018245.2:c.1318C>T (OGDHL))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.50954002G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID OGDHL_000011 See all 2 reported entries
Variant remarks Variant functionally tested and re-classified
Reference Journal: Lin 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Barbara Vona
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Barbara Vona
Date created 2022-02-13 18:12:08 +01:00 (CET)
Date last edited 2023-11-20 06:57:29 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGDHL NM_018245.2 +/. - c.1318C>T r.(?) p.(Arg440*)


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