Variant #0001291338 (NC_000013.10:g.95847194A>G, NC_000013.10(NM_005845.3):c.1162-3T>C (ABCC4))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.95847194A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC4_000211
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
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 16:41:01 +02:00 (CEST)
Date last edited 2018-08-23 13:18:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC4 NM_005845.3 ?/? c.1162-3T>C r.spl? p.?