Variant #0000447037 (NC_000009.11:g.119461202G>A, NM_012210.3:c.1181G>A (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.119461202G>A |
| DNA change (hg38) |
g.116698923G>A |
| Published as |
1180G>A |
| ISCN |
- |
| DB-ID |
TRIM32_000009 See all 7 reported entries |
| Variant remarks |
YTH cloning in pGBKT7/pGADT7, no homo-dimerisation, no 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) |
4.0E-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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