Variant #0000036171 (NC_000009.11:g.132581031A>T, NM_000113.2:c.613T>A (TOR1A))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.132581031A>T |
| DNA change (hg38) |
g.129818752A>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TOR1A_000009 See all 2 reported entries |
| Variant remarks |
GFP-fusion expression cloning BHK cells, significantly increased intracellular inclusion bodies |
| Reference |
PubMed: Calakos 2010 |
| 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 |
2014-04-15 21:55:43 +02:00 (CEST) |
| Date last edited |
2025-01-03 15:17:47 +01:00 (CET) |

Variant on transcripts
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