Variant #0000439304 (NC_000002.11:g.220283543C>A, NM_001927.3:c.359C>A (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.220283543C>A |
| DNA change (hg38) |
g.219418821C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DES_000069 See all 2 reported entries |
| Variant remarks |
expression cloning shows severe filament formation defect giving cytoplasmic aggregates; tested also A120L, A120V, A120E, A120R and A120K |
| Reference |
PubMed: Brodehl 2013 |
| 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 |
2014-01-25 12:59:09 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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