Variant #0000693784 (NC_000009.11:g.135819931_135820009del, NC_000009.11(NM_000368.4):c.-219_-144+3del (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.135819931_135820009del
DNA change (hg38) g.132944544_132944622del
Published as -
ISCN -
DB-ID TSC1_001471 See all 2 reported entries
Variant remarks 79bp deletion extends from exon 1 to intron 1; deletion extends into the promoter region which starts in exon 1 and is reported to be between nts. -157bp and -744bp; promoter region partially deleted. Effect on gene expression not determined.
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site AluI-, BanI-
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 2020-09-15 23:30:13 +02:00 (CEST)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
Options




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.-219_-144+3del r.0? p.0? - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.