Variant #0000949242 (NC_000009.11:g.135782083G>C, NC_000009.11(NM_000368.4):c.1438+35C>G (TSC1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.135782083G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC1_000083
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 06:04:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC1 NM_000368.4 ?/? c.1438+35C>G r.(=) p.(=)