Variant #0000186905 (NC_000001.10:g.229654011T>G, NM_012089.2:c.2132A>C (ABCB10))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.229654011T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB10_000006
Frequency 1/13000
Freq. EA 1/8594
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 16:20:35 +02:00 (CEST)
Date last edited 2018-08-23 01:29:47 +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.2132A>C r.(?) p.(Glu711Ala)