Variant #0001608547 (NC_000017.10:g.48736561T>G, NC_000017.10(NM_001144070.1):c.675-37T>G (ABCC3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48736561T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC3_000059
Frequency 27/13006
Freq. EA 0/8600
Freq. AA 27/4406
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 2018-08-23 04:29:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC3 NM_001144070.1 ?/? c.675-37T>G r.(=) p.(=)