Variant #0000469442 (NC_000009.11:g.(135787845_135796749)_(135804340_135810419)del, NC_000009.11(NM_000368.4):c.(-81+1_-80-1)_(737+1_738-1)del (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(135787845_135796749)_(135804340_135810419)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC1_000782 See all 2 reported entries
Variant remarks exons 3-8 deleted
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
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 2019-03-15 13:22:37 +01:00 (CET)
Date last edited 2020-11-02 09:56:34 +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 +?/+? 2i_8i c.(-81+1_-80-1)_(737+1_738-1)del r.? p.? - -


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