Variant #0000699449 (NC_000009.11:g.135798749C>T, NM_000368.4:c.494G>A (TSC1))

Chromosome 9
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.135798749C>T
DNA change (hg38) g.132923362C>T
Published as p.C165Y
ISCN -
DB-ID TSC1_000912 See all 3 reported entries
Variant remarks T389/S6K ratio significantly increased compared to wild-type TSC2; TSC complex function disrupted
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 Mark Nellist
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-11-02 10:52:17 +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     
TSC1 NM_000368.4 +?/. 6 c.494G>A - p.Cys165Tyr Rho-activating domain -


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