Variant #0001861029 (NC_000020.10:g.49458479C>G, NC_000020.10(NM_017843.3):c.489+42C>G (BCAS4))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.49458479C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCAS4_000035
Frequency 321/13000
Freq. EA 86/8594
Freq. AA 235/4406
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 2019-04-09 20:50:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCAS4 NM_017843.3 ?/? c.489+42C>G r.(=) p.(=)