Variant #0001449026 (NC_000016.9:g.2103379C>T, NM_000548.3:c.262C>T (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2103379C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000021
Frequency 10/12954
Freq. EA 0/8578
Freq. AA 10/4376
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 08:34:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC2 NM_000548.3 ?/? c.262C>T r.(=) p.(=)