Variant #0000839740 (NC_000010.10:g.50953856A>G, NM_018245.2:c.1464T>C (OGDHL))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50953856A>G |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
OGDHL_000010 See all 2 reported entries |
Variant remarks |
- |
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 18:03:58 +01:00 (CET) |
Date last edited |
2023-11-20 06:48:56 +01:00 (CET) |

Variant on transcripts
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