Variant #0000699441 (NC_000009.11:g.135800997G>A, NM_000368.4:c.340C>T (TSC1))
Chromosome |
9 |
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.135800997G>A |
DNA change (hg38) |
g.132925610G>A |
Published as |
p.P114S |
ISCN |
- |
DB-ID |
TSC1_000969 See all 4 reported entries |
Variant remarks |
T389/S6K ratio significantly increased compared to wild-type TSC2; TSC complex function disrupted |
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) |
1.0E-5 View details |
Owner |
Mark Nellist |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2020-11-02 10:52:17 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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