Variant #0000598254 (NC_000016.9:g.(?_2098587)_(2136873_2137863)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(4989+1_4990-1)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)_(2136873_2137863)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_002692 See all 4 reported entries
Variant remarks exons 2-38 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 2019-10-12 14:26:04 +02:00 (CEST)
Date last edited 2021-08-18 14:44:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1i_38i c.(?_-29-1)_(4989+1_4990-1)del r.? p.? - -


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