Variant #0001608562 (NC_000017.10:g.48738266C>T, NC_000017.10(NM_001144070.1):c.807-18C>T (ABCC3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.48738266C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC3_000074
Frequency 1118/13006
Freq. EA 802/8600
Freq. AA 316/4406
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 11:19:43 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC3 NM_001144070.1 ?/? c.807-18C>T r.(=) p.(=)