Variant #0000592785 (NC_000021.8:g.44483098C>T, NM_000071.2:c.919G>A (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.44483098C>T |
DNA change (hg38) |
g.43062988C>T |
Published as |
- |
ISCN |
- |
DB-ID |
CBS_000122 See all 79 reported entries |
Variant remarks |
expression cloning in E.coli, CBs activity 0 |
Reference |
PubMed: Hu 1993 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00015 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 22:28:19 +02:00 (CEST) |

Variant on transcripts
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