Variant #0001606090 (NC_000017.10:g.48190207G>A, NM_174920.3:c.*50C>T (SAMD14))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48190207G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD14_000001
Frequency 1/12904
Freq. EA 1/8528
Freq. AA 0/4376
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 18:15:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD14 NM_174920.3 ?/? c.*50C>T r.(=) p.(=)