Variant #0001449090 (NC_000016.9:g.2107099C>G, NC_000016.9(NM_000548.3):c.775-7C>G (TSC2))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2107099C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC2_000085
Frequency 1/12104
Freq. EA 1/7962
Freq. AA 0/4142
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 07:06:17 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC2 NM_000548.3 ?/? c.775-7C>G r.(=) p.(=)