Variant #0000949312 (NC_000009.11:g.135801136_135801137insA, NC_000009.11(NM_000368.4):c.211-11_211-10insT (TSC1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.135801136_135801137insA
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC1_000151
Frequency 1/12518
Freq. EA 1/8254
Freq. AA 0/4264
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 2021-07-25 21:42:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC1 NM_000368.4 ?/? c.211-11_211-10insT r.(=) p.(=)