Variant #0000871280 (NC_000008.10:g.144512446C>T, NM_201589.3:c.131G>A (MAFA))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.144512446C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAFA_000018
Frequency 1/12762
Freq. EA 1/8466
Freq. AA 0/4296
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 15:49:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAFA NM_201589.3 ?/? c.131G>A r.(?) p.(Arg44His)