Variant #0000629917 (NC_000016.9:g.2137923_2137924insGG, NM_000548.3:c.5049_5050insGG (TSC2))

Chromosome 16
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.2137923_2137924insGG
DNA change (hg38) g.2087922_2087923insGG
Published as -
ISCN -
DB-ID TSC2_001293 See all 2 reported entries
Variant remarks 2bp insertion of GG; protein extends beyond stop codon
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site AvaII+, Sau96I+
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 2020-01-02 10:22:42 +01:00 (CET)
Date last edited 2022-01-23 23:19:04 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 ?/? 39 c.5049_5050insGG r.(?) p.(Ser1684Glyfs*143) Gap domain -


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