Variant #0000455566 (NC_000009.11:g.135786868G>A, NM_000368.4:c.1001C>T (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.135786868G>A |
DNA change (hg38) |
g.132911481G>A |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000279 See all 8 reported entries |
Variant remarks |
did not affect TSC1 function; TSC1 levels as wild-type; S6K T389 phosphorylation not significantly higher than wild type TSC1, but is significantly lower than pathogenic TSC1 variant; variant formed large cytoplasmic aggregates which reduced in number when TSC2 coexpressed; reported as non-pathogenic/probably neutral |
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) |
0.00043 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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