Variant #0001608498 (NC_000017.10:g.48733288C>T, NM_001144070.1:c.141C>T (ABCC3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48733288C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC3_000010
Frequency 17/13006
Freq. EA 13/8600
Freq. AA 4/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2024-04-28 11:39:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC3 NM_001144070.1 ?/? c.141C>T r.(=) p.(=)