Variant #0001246748 (NC_000012.11:g.112892525T>G, NC_000012.11(NM_002834.3):c.642+41T>G (PTPN11))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.112892525T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTPN11_000018
Frequency 2/13004
Freq. EA 2/8598
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 2016-02-17 18:22:35 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTPN11 NM_002834.3 ?/? c.642+41T>G r.(=) p.(=)