Variant #0001006614 (NC_000010.10:g.88719758T>C, NM_003087.2:c.164T>C (SNCG))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.88719758T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SNCG_000014
Frequency 16/12984
Freq. EA 13/8596
Freq. AA 3/4388
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 19:55:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SNCG NM_003087.2 ?/? c.164T>C r.(?) p.(Val55Ala)