Variant #0000455569 (NC_000009.11:g.135786002C>T, NM_000368.4:c.1219G>A (TSC1))
| Chromosome |
9 |
| 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.135786002C>T |
| DNA change (hg38) |
g.132910615C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000577 See all 3 reported entries |
| Variant remarks |
reported that TSC1 stability and TSC1-TSC2 interaction unaffected, effective inhibition of TORC1; concluded that no evidence for an effect on TSC complex activity |
| 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) |
3.0E-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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