Variant #0000447040 (NC_000009.11:g.119460409C>T, NM_012210.3:c.388C>T (TRIM32))
Chromosome |
9 |
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.119460409C>T |
DNA change (hg38) |
g.116698130C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TRIM32_000007 See all 3 reported entries |
Variant remarks |
YTH cloning in pGBKT7/pGADT7, normal homo-dimerisation, normal UBE2N binding; GFP-TRIM32 normal localization COS7 |
Reference |
PubMed: Saccone 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2008-07-18 17:05:06 +02:00 (CEST) |
Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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