Variant #0000782119 (NC_000016.9:g.(?_2098587)_(2135324_2136193)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(4662+1_4663-1)del (TSC2))

Chromosome 16
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.(?_2098587)_(2135324_2136193)del
DNA change (hg38) g.(?_2048586)_(2085323_2086192)del
Published as -
ISCN -
DB-ID TSC2_003269 See all 2 reported entries
Variant remarks exons 2-36 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 2021-05-04 16:22:13 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1i_36i c.(?_-29-1)_(4662+1_4663-1)del r.? p.? - -


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