Variant #0000455576 (NC_000009.11:g.135802649A>G, NM_000368.4:c.149T>C (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.135802649A>G
DNA change (hg38) g.132927262A>G
Published as -
ISCN -
DB-ID TSC1_000005 See all 7 reported entries
Variant remarks TSC1 function affected; phosphorylation of S6K T389 significantly higher than wild type TSC1; reduced TSC1 levels (significantly less than wild type) due to degradation by proteosome as seen by MG-132 treatment; steady state expression of variant reduced therefore variant unstable; variant expressed uniformly (diffuse) in cytoplasm even when TSC2 coexpressed
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) Retrieve
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)
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Variant on transcripts


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AscendingTranscript     

Affects function     

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DNA change (cDNA)     

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Protein     

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Predict-BioInf     
TSC1 NM_000368.4 +?/. 4 c.149T>C - p.Leu50Pro - -


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