Variant #0000839747 (NC_000010.10:g.50958886T>C, NM_018245.2:c.895A>G (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.50958886T>C |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
OGDHL_000013 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 International |
| Created by |
Barbara Vona |
| Date created |
2022-02-13 18:11:06 +01:00 (CET) |
| Date last edited |
2023-11-20 06:59:45 +01:00 (CET) |

Variant on transcripts
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