Variant #0000442353 (NC_000003.11:g.183689332C>G, NC_000003.11(NM_005688.2):c.1761+19G>C (ABCC5))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183689332C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC5_000158
Frequency 44/12478
Freq. EA 1/8374
Freq. AA 43/4104
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 16:23:53 +02:00 (CEST)
Date last edited 2018-08-23 10:09:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC5 NM_005688.2 ?/? c.1761+19G>C r.(=) p.(=)