Variant #0000808224 (NC_000007.13:g.156801687G>T, NC_000007.13(NM_001165255.1):c.55+5C>A (MNX1))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.156801687G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MNX1_000011
Frequency 33/4566
Freq. EA 32/3182
Freq. AA 1/1384
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 13:58:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MNX1 NM_001165255.1 ?/? c.55+5C>A r.spl? p.?