Variant #0001449031 (NC_000016.9:g.2103415G>A, NM_000548.3:c.298G>A (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2103415G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000026
Frequency 1/12954
Freq. EA 0/8570
Freq. AA 1/4384
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:42:42 +02:00 (CEST)
Date last edited 2018-08-23 07:05:36 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC2 NM_000548.3 ?/? c.298G>A r.(?) p.(Ala100Thr)