Variant #0001449029 (NC_000016.9:g.2103399G>A, NM_000548.3:c.282G>A (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2103399G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000024
Frequency 1/12960
Freq. EA 1/8580
Freq. AA 0/4380
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 2019-10-11 15:22:35 +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.282G>A r.(=) p.(=)