Variant #0000709118 (NC_000016.9:g.2124214_2124216del, NM_000548.3:c.2369_2371del (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.2124214_2124216del
DNA change (hg38) g.2074213_2074215del
Published as (p.790del)
ISCN -
DB-ID TSC2_001158 See all 3 reported entries
Variant remarks variant inactivates the TSC complex; T389/S6K ratio significantly increased compared to wild-type TSC2, TSC1 signal significantly decreased; no inhibition of TORC1
Reference Nellist, personal communication
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 2020-12-24 09:47:49 +01:00 (CET)
Date last edited N/A
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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 +/. 22 c.2369_2371del - p.Tyr790del Hamartin binding domain -


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