Variant #0000498503 (NC_000005.9:g.125929086G>T, NM_001182.4:c.203C>A (ALDH7A1))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.125929086G>T |
| DNA change (hg38) |
g.126593394G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ALDH7A1_000151 See all 2 reported entries |
| Variant remarks |
expression cloning in E.coli (at 37oC) shows 0.535 alpha‐AASADH activity (nmol NADH/min/mg ATQ) |
| Reference |
PubMed: Coughlin 2019 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00011 View details |
| Owner |
Curtis Coughlin II |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-06-11 17:50:42 +02:00 (CEST) |
| Date last edited |
2020-06-17 14:49:33 +02:00 (CEST) |

Variant on transcripts
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