Variant #0000670909 (NC_000006.11:g.24502767T>G, NM_001080.3:c.371T>G (ALDH5A1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24502767T>G |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ALDH5A1_006150 |
| Variant remarks |
overexpression in HEK293 cells showed severely impaired SSADH activity (below 15%) |
| Reference |
PubMed: Popp 2020, Journal: Pop 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Gajja Salomons |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-07-02 16:49:46 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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