Variant #0001606111 (NC_000017.10:g.48191422G>C, NM_174920.3:c.1048C>G (SAMD14))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48191422G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD14_000022
Frequency 3/12992
Freq. EA 2/8592
Freq. AA 1/4400
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 18:15:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD14 NM_174920.3 ?/? c.1048C>G r.(?) p.(Pro350Ala)