Variant #0000839739 (NC_000010.10:g.50948878C>T, NM_018245.2:c.2018G>A (OGDHL))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS (!)
DNA change (genomic) (Relative to hg19 / GRCh37) g.50948878C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID OGDHL_000007 See all 2 reported entries
Variant remarks Variant functionally tested and re-classified as VUS-favor pathogenic
Reference Journal: Lin 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Barbara Vona
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Barbara Vona
Date created 2022-02-13 18:02:17 +01:00 (CET)
Date last edited 2023-11-20 07:05:05 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGDHL NM_018245.2 +?/. - c.2018G>A r.(?) p.(Arg673Gln)


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