Variant #0000684087 (NC_000016.9:g.2138453G>A, NM_000548.3:c.5266G>A (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2138453G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_004243 See all 5 reported entries |
Variant remarks |
TSC1 and TSC2 signals, and T389/S6K ratio are not significantly different compared to wild type TSC2; variant did not disrupt TSC2 function in vitro |
Reference |
Nellist, personal communication |
ClinVar ID |
- |
dbSNP ID |
rs375075952 |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2020-08-26 09:13:20 +02:00 (CEST) |
Date last edited |
2020-12-02 11:06:02 +01:00 (CET) |

Variant on transcripts
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