Variant #0001449091 (NC_000016.9:g.2107112C>T, NM_000548.3:c.781C>T (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2107112C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000086
Frequency 1/12130
Freq. EA 1/7974
Freq. AA 0/4156
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 07:00:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC2 NM_000548.3 ?/? c.781C>T r.(?) p.(Arg261Trp)