Variant #0001606156 (NC_000017.10:g.48193410_48193412del, NM_174920.3:c.542_544del (SAMD14))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48193410_48193412del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD14_000067
Frequency 1/12518
Freq. EA 1/8254
Freq. AA 0/4264
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 18:15:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD14 NM_174920.3 ?/? c.542_544del r.(?) p.(Thr181del)