Variant #0000164261 (NC_000001.10:g.202122811C>T, NC_000001.10(NM_002832.3):c.1032+42G>A (PTPN7))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.202122811C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTPN7_000050
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 20:41:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTPN7 NM_002832.3 ?/? c.1032+42G>A r.(=) p.(=)