Variant #0000455947 (NC_000016.9:g.2098619G>A, NM_000548.3:c.3G>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.2098619G>A
DNA change (hg38) g.2048618G>A
Published as -
ISCN -
DB-ID TSC2_002080 See all 3 reported entries
Variant remarks no significant difference in TSC1 signal; TSC2 signals significantly reduced compared to wild-type TSC2 indicating aa change destabilises TSC2 causing accelerated degradation of variant; mean T389/S6K ratio of variant significantly higher than that of wild-type TSC2 and not different from that of pathogenic TSC2 p.R611Q indicating variant was less effective at inhibiting TORC1
Reference PubMed: Hoogeveen-Westerveld, 2013
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)
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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 +/. 2 c.3G>A - p.0? Hamartin binding domain -


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