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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 -?/. 10 c.1001C>T - p.Ser334Leu Tuberin binding domain -


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