Variant #0000122138 (NC_000001.10:g.153933082G>A, NM_014437.3:c.467C>T (SLC39A1))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.153933082G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLC39A1_000016
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 19:42:53 +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.467C>T r.(?) p.(Pro156Leu)