Variant #0000804653 (NC_000007.13:g.150916256A>G, NC_000007.13(NM_005692.3):c.922-11T>C (ABCF2))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.150916256A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCF2_000071
Frequency 1/13006
Freq. EA 1/8600
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 00:03:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCF2 NM_005692.3 ?/? c.922-11T>C r.(=) p.(=)