Variant #0000684087 (NC_000016.9:g.2138453G>A, NM_000548.3:c.5266G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.2138453G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_004243 See all 5 reported entries
Variant remarks TSC1 and TSC2 signals, and T389/S6K ratio are not significantly different compared to wild type TSC2; variant did not disrupt TSC2 function in vitro
Reference Nellist, personal communication
ClinVar ID -
dbSNP ID rs375075952
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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 09:13:20 +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 -?/. 42 c.5266G>A - p.Glu1756Lys GAP domain -


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