Variant #0001848427 (NC_000020.10:g.36151101C>G, NC_000020.10(NM_006698.3):c.-176-3349G>C (BLCAP))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.36151101C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BLCAP_000024
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 16:46:43 +02:00 (CEST)
Date last edited 2013-05-06 04:46:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NNAT NM_005386.2 ?/? c.186C>G r.(?) p.(Tyr62*)
BLCAP NM_006698.3 ?/? c.-176-3349G>C r.(?) p.(Tyr62*)