Variant #0000779774 (NC_000007.13:g.116339672C>T, NM_000245.2:c.534C>T (MET))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.116339672C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MET_000037
Frequency 851/12216
Freq. EA 337/8286
Freq. AA 514/3930
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 13:09:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MET NM_000245.2 ?/? c.534C>T r.(=) p.(=)