Variant #0000122131 (NC_000001.10:g.153932927T>C, NM_014437.3:c.622A>G (SLC39A1))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.153932927T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLC39A1_000002
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 19:42:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A1 NM_014437.3 ?/? c.622A>G r.(?) p.(Met208Val)