Variant #0000439327 (NC_000002.11:g.220286087G>C, NM_001927.3:c.1049G>C (DES))
| Chromosome |
2 |
| 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.220286087G>C |
| DNA change (hg38) |
g.219421365G>C |
| Published as |
R350P |
| ISCN |
- |
| DB-ID |
DES_000030 See all 17 reported entries |
| Variant remarks |
cloned in pIRES GFP-DES, expressed in SW-13, BMGE cells; cytoplasmic aggregates |
| Reference |
PubMed: Bar 2005, PubMed: Walter 2007, OMIM:var0016 |
| 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 |
2008-06-20 20:39:37 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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