Variant #0000684382 (NC_000016.9:g.2108798G>T, NM_000548.3:c.899G>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.2108798G>T
DNA change (hg38) g.2058797G>T
Published as -
ISCN -
DB-ID TSC2_001259 See all 6 reported entries
Variant remarks TSC1 signal significantly reduced but no significant change in TSC2 signal; T389/S6K ratio significantly increased compared to wildtype TSC2 but significantly reduced compared to pathogenic TSC2 c.1832G>A (p.Arg611Gln) indicating reduced activity of the TSC complex
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 2020-08-26 10:25:17 +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 +?/. 10 c.899G>T - p.Gly300Val Hamartin binding domain -


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