Variant #0001246749 (NC_000012.11:g.112892526_112892530del, NC_000012.11(NM_002834.3):c.642+42_642+46del (PTPN11))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.112892526_112892530del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTPN11_000020
Frequency 5/12514
Freq. EA 0/8252
Freq. AA 5/4262
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 04:28:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTPN11 NM_002834.3 ?/? c.642+42_642+46del r.(=) p.(=)