Variant #0001681409 (NC_000019.9:g.306647G>A, NM_017550.1:c.*43C>T (MIER2))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.306647G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MIER2_000003
Frequency 1/12216
Freq. EA 1/8066
Freq. AA 0/4150
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 16:45:39 +02:00 (CEST)
Date last edited 2014-05-01 03:25:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MIER2 NM_017550.1 ?/? c.*43C>T r.(=) p.(=)