Variant #0000456061 (NC_000016.9:g.2107170T>C, NM_000548.3:c.839T>C (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.2107170T>C
DNA change (hg38) g.2057169T>C
Published as -
ISCN -
DB-ID TSC2_002785 See all 4 reported entries
Variant remarks variant retained some activity; shows significantly increased T389/S6K ratio compared to wild-type TSC2 but significantly reduced compared to pathogenic TSC2 R611Q; variant affects TSC1-TSC2 interaction and disrupts TSC2 complex function; Met280Thr causes packing defect; likely pathogenic
Reference PubMed: Dufner Almeida 2020
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 2015-07-22 03:06:15 +02:00 (CEST)
Date last edited 2021-04-23 13:58:39 +02:00 (CEST)
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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 +/. 9 c.839T>C - p.Met280Thr Hamartin binding domain -


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