Variant #0000456050 (NC_000016.9:g.2106652T>C, NM_000548.3:c.656T>C (TSC2))
| Chromosome |
16 |
| 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.2106652T>C |
| DNA change (hg38) |
g.2056651T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_002012 See all 7 reported entries |
| Variant remarks |
phosphorylation of S6K T389 significantly higher than wild type TSC2; significant reduction in TSC1 signal hence destabilising |
| Reference |
PubMed: Hoogeveen-Westerveld, 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2013-06-12 02:25:54 +02:00 (CEST) |
| Date last edited |
2021-04-23 13:58:39 +02:00 (CEST) |

Variant on transcripts
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