Variant #0000949230 (NC_000009.11:g.135781264C>T, NM_000368.4:c.1701G>A (TSC1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.135781264C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC1_000069
Frequency 24/13006
Freq. EA 0/8600
Freq. AA 24/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2018-08-23 06:03:07 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC1 NM_000368.4 ?/? c.1701G>A r.(=) p.(=)