Variant #0000634452 (NC_000006.11:g.30551693C>T, NC_000006.11(NM_001025091.1):c.1102+26C>T (ABCF1))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.30551693C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCF1_000074
Frequency 2/8440
Freq. EA 2/5418
Freq. AA 0/3022
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 16:27:59 +02:00 (CEST)
Date last edited 2018-08-23 12:34:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCF1 NM_001025091.1 ?/? c.1102+26C>T r.(=) p.(=)