Variant #0000047592 (NC_000001.10:g.32165639C>T, NC_000001.10(NM_001856.3):c.148+3G>A (COL16A1))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.32165639C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID COL16A1_000523
Frequency 1/12878
Freq. EA 1/8518
Freq. AA 0/4360
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 18:01:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
COL16A1 NM_001856.3 ?/? c.148+3G>A r.spl? p.?