Variant #0000670908 (NC_000006.11:g.24495578G>C, NM_001080.3:c.354G>C (ALDH5A1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24495578G>C |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ALDH5A1_006149 |
| Variant remarks |
overexpression in HEK293 cells showed normal SSADH activity. This variant may affect splicing. |
| 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) |
1.0E-5 View details |
| 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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