Variant #0000498520 (NC_000005.9:g.125918566C>T, NM_001182.4:c.494G>T (ALDH7A1))
Chromosome |
5 |
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.125918566C>T |
DNA change (hg38) |
g.126582874C>T |
Published as |
- |
ISCN |
- |
DB-ID |
ALDH7A1_000135 See all 2 reported entries |
Variant remarks |
expression cloning in E.coli shows no alpha‐AASADH activity Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. |
Reference |
PubMed: Korasick 2017 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
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 |
N/A |

Variant on transcripts
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