Variant #0000455450 (NC_000001.10:g.26384973G>A, NM_032588.3:c.739C>T (TRIM63))
| Chromosome |
1 |
| 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.26384973G>A |
| DNA change (hg38) |
g.26058482G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TRIM63_000011 See all 11 reported entries |
| Variant remarks |
FLAG-tagged cDNA expression cloning and co-IP in HeLa cells showed near complete loss of autoubiquitination; other assays performed as well |
| Reference |
PubMed: Chen 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00066 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-02-09 22:28:23 +01:00 (CET) |
| Date last edited |
2020-06-04 09:32:41 +02:00 (CEST) |

Variant on transcripts
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