Variant #0000674778 (NC_000009.11:g.(135782758_135785957)_(135766735_?)del, NM_000368.4:c.(1263+1_1264-1)_*4887{0} (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(135782758_135785957)_(135766735_?)del
DNA change (hg38) g.(132907371_132910570)_(132891348_?)del
Published as -
ISCN -
DB-ID TSC1_001414 See all 2 reported entries
Variant remarks exons 13-23 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 2020-07-20 14:30:39 +02:00 (CEST)
Date last edited 2020-07-20 14:32:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 +/+ 12i_23_ c.(1263+1_1264-1)_*4887{0} r.? p.? - -


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