Variant #0000709124 (NC_000016.9:g.2124385T>C, NM_000548.3:c.2540T>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.2124385T>C |
DNA change (hg38) |
g.2074384T>C |
Published as |
(p.L847P) |
ISCN |
- |
DB-ID |
TSC2_000466 See all 8 reported entries |
Variant remarks |
variant inactivates the TSC complex; TSC1 and TSC2 signals significantly reduced; T389/S6K ratio significantly increased compared to wild-type TSC2; no inhibition of TORC1 |
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 |
2020-12-24 09:47:49 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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