Variant #0000186992 (NC_000001.10:g.229684976G>A, NC_000001.10(NM_012089.2):c.718+5C>T (ABCB10))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.229684976G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB10_000093
Frequency 5/13006
Freq. EA 0/8600
Freq. AA 5/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2018-08-23 10:22:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB10 NM_012089.2 ?/? c.718+5C>T r.spl? p.?