Variant #0000455932 (NC_000016.9:g.2130366C>T, NM_000548.3:c.3598C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.2130366C>T
DNA change (hg38) g.2080365C>T
Published as -
ISCN -
DB-ID TSC2_000056 See all 36 reported entries
Variant remarks assay using TSC2 null cells showed T389/S6K ratio significantly increased compared to wild type TSC2 and the same as the pathogenic TSC2 R611Q variant; TSC1 and TSC2 signals significantly reduced compared to wild type TSC2; variant disrupts TSC2 function
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 Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2015-08-20 07:01:16 +02:00 (CEST)
Date last edited 2020-12-02 11:06:02 +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     
TSC2 NM_000548.3 +/. 30 c.3598C>T - p.Arg1200Trp - -


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