Variant #0000592007 (NC_000009.11:g.(135810483_135819929)_(135820020_?)del, NC_000009.11(NM_000368.4):c.(?_-234)_(-144+1_-143-1)del (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(135810483_135819929)_(135820020_?)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC1_000512 See all 11 reported entries
Variant remarks TSC1 exon 1 and at least 23kb upstream deleted; deletion removes the promoter region reported between nts. -157bp and -744bp
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
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 2019-08-07 16:14:03 +02:00 (CEST)
Date last edited 2020-08-15 20:04:04 +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     
TSC1 NM_000368.4 +/. _1_1i c.(?_-234)_(-144+1_-143-1)del r.0? p.0? - -


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