Variant #0000592768 (NC_000021.8:g.[44488629C>G;44488702G>C], NM_000071.2:c.[233C>G;306G>C] (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.[44488629C>G;44488702G>C] |
| DNA change (hg38) |
g.[43068519C>G;43068592G>C] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CBS_000058 |
| Variant remarks |
expression cloning in E.coli, CBs activity 0 |
| Reference |
PubMed: de Franchis 1994 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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 |
2019-08-16 14:06:09 +02:00 (CEST) |

Variant on transcripts
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