Variant #0000592770 (NC_000021.8:g.44486463G>A, NM_000071.2:c.341C>T (CBS))
Chromosome |
21 |
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.44486463G>A |
DNA change (hg38) |
g.43066353G>A |
Published as |
- |
ISCN |
- |
DB-ID |
CBS_000199 See all 24 reported entries |
Variant remarks |
expression cloning in E.coli, CBs activity 0-0.545 |
Reference |
PubMed: Kozich 1993, PubMed: de Franchis 1999 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00021 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-08-16 14:04:43 +02:00 (CEST) |
Date last edited |
2020-07-16 22:29:46 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|