Variant #0000839742 (NC_000010.10:g.50957779G>A, NM_018245.2:c.980C>T (OGDHL))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.50957779G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID OGDHL_000012 See all 3 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) Retrieve
Owner Barbara Vona
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Barbara Vona
Date created 2022-02-13 18:06:13 +01:00 (CET)
Date last edited 2023-11-20 06:51:18 +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.980C>T r.(?) p.(Ala327Val)


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