Variant #0000709067 (NC_000016.9:g.2106700G>A, NM_000548.3:c.704G>A (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2106700G>A |
DNA change (hg38) |
g.2056699G>A |
Published as |
(p.S235N) |
ISCN |
- |
DB-ID |
TSC2_001216 See all 4 reported entries |
Variant remarks |
variant did not disrupt TSC2 function in vitro (TSC complex active); TSC1 and TSC2 signals, and T389/S6K ratio are not significantly different compared to wild type TSC2 |
Reference |
PubMed: Hoogeveen-Westerveld, 2013 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2020-12-24 09:47:49 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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