Variant #0000455936 (NC_000016.9:g.2131596G>A, NM_000548.3:c.3611G>A (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.2131596G>A
DNA change (hg38) g.2081595G>A
Published as -
ISCN -
DB-ID TSC2_000885 See all 6 reported entries
Variant remarks phosphorylation of S6K T389 significantly higher than wild type TSC2
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 2013-06-12 02:25:54 +02:00 (CEST)
Date last edited 2021-04-23 13:58:39 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/. 31 c.3611G>A - p.Gly1204Glu - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.