Variant #0000795558 (NC_000016.9:g.2134963T>C, NM_000548.3:c.4505T>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.2134963T>C |
| DNA change (hg38) |
g.2084962T>C |
| Published as |
p.L1502P |
| ISCN |
- |
| DB-ID |
TSC2_001628 See all 4 reported entries |
| Variant remarks |
TSC2 stability and TSC1-TSC2 interaction unaffected; no inhibition of TORC1; TSC complex inactivated |
| 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 |
Mark Nellist |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2021-08-23 10:50:38 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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