Variant #0001615064 (NC_000017.10:g.58767136del, NC_000017.10(NM_017679.3):c.214+14del (BCAS3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.58767136del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCAS3_000008
Frequency 6/11282
Freq. EA 2/7794
Freq. AA 4/3488
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 18:39:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCAS3 NM_017679.3 ?/? c.214+14del r.(=) p.(=)