Variant #0000455453 (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 09:32:42 +02:00 (CEST) |

Variant on transcripts
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