Variant #0001105687 (NC_000011.9:g.64573779G>A, NM_000244.3:c.989C>T (MEN1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.64573779G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MEN1_000031
Frequency 1/12996
Freq. EA 1/8594
Freq. AA 0/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2016-06-20 18:36:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MEN1 NM_000244.3 ?/? c.989C>T r.(?) p.(Ala330Val)