Variant #0001848430 (NC_000020.10:g.36151165C>T, NC_000020.10(NM_006698.3):c.-176-3413G>A (BLCAP))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.36151165C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BLCAP_000027
Frequency 1/12962
Freq. EA 1/8576
Freq. AA 0/4386
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.*4C>T r.(=) p.(=)
BLCAP NM_006698.3 ?/? c.-176-3413G>A r.(=) p.(=)