Variant #0001246794 (NC_000012.11:g.112940030C>T, NM_002834.3:c.1682C>T (PTPN11))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.112940030C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTPN11_000071
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 04:28:20 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTPN11 NM_002834.3 ?/? c.1682C>T r.(?) p.(Pro561Leu)