Variant #0000455633 (NC_000009.11:g.135798846C>T, NM_000368.4:c.397G>A (TSC1))
| Chromosome |
9 |
| 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.135798846C>T |
| DNA change (hg38) |
g.132923459C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000466 See all 3 reported entries |
| Variant remarks |
TSC2 expression/stability not significantly affected by TSC1 variant; same TSC1 protein levels, reduced S6K T389 phosphorylation and large cytoplasmic TSC1 protein aggregates as wild type TSC1 |
| Reference |
PubMed: Hoogeveen-Westerveld, 2011 |
| 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 |
No license selected |
| Created by |
Mark Nellist |
| Date created |
2018-05-24 22:32:24 +02:00 (CEST) |
| Date last edited |
2020-11-02 09:36:38 +01:00 (CET) |

Variant on transcripts
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