Variant #0000455954 (NC_000016.9:g.2134372C>T, NM_000548.3:c.4149C>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.2134372C>T
DNA change (hg38) g.2084371C>T
Published as -
ISCN -
DB-ID TSC2_003348 See all 4 reported entries
Variant remarks mTOR activity partially reduced in patientís normal skin but activated in affected skin; variant affects mTOR activity
Reference PubMed: Møller, 2017
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 2018-05-24 23:01:25 +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 +/. 34 c.4149C>T - p.Ser1383fs* - -


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