Variant #0000839744 (NC_000010.10:g.50953848T>A, NM_018245.2:c.1472A>T (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.50953848T>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
OGDHL_000009 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) |
0 View details |
Owner |
Barbara Vona |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Barbara Vona |
Date created |
2022-02-13 18:08:07 +01:00 (CET) |
Date last edited |
2023-11-20 07:02:16 +01:00 (CET) |

Variant on transcripts
|