Variant #0001017812 (NC_000010.10:g.101554146T>G, NC_000010.10(NM_000392.3):c.577-24T>G (ABCC2))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.101554146T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC2_000052
Frequency 6/13006
Freq. EA 6/8600
Freq. AA 0/4406
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 16:30:47 +02:00 (CEST)
Date last edited 2018-08-23 07:24:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC2 NM_000392.3 ?/? c.577-24T>G r.(=) p.(=)