Variant #0000684382 (NC_000016.9:g.2108798G>T, NM_000548.3:c.899G>T (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2108798G>T |
| DNA change (hg38) |
g.2058797G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001259 See all 6 reported entries |
| Variant remarks |
TSC1 signal significantly reduced but no significant change in TSC2 signal; T389/S6K ratio significantly increased compared to wildtype TSC2 but significantly reduced compared to pathogenic TSC2 c.1832G>A (p.Arg611Gln) indicating reduced activity of the TSC complex |
| Reference |
Nellist, personal communication |
| 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 |
2020-08-26 10:25:17 +02:00 (CEST) |
| Date last edited |
2020-12-02 11:06:02 +01:00 (CET) |

Variant on transcripts
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