Variant #0001449057 (NC_000016.9:g.2105553T>C, NC_000016.9(NM_000548.3):c.599+33T>C (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2105553T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000052
Frequency 1/12996
Freq. EA 0/8600
Freq. AA 1/4396
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 07:09:21 +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.599+33T>C r.(=) p.(=)