Variant #0001974696 (NC_000023.10:g.74290148T>C, NC_000023.10(NM_004299.3):c.1368+52A>G (ABCB7))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.74290148T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB7_000021
Frequency 4/4525
Freq. EA 0/3107
Freq. AA 4/1418
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 16:50:35 +02:00 (CEST)
Date last edited 2018-08-23 10:27:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_004299.3 ?/? c.1368+52A>G r.(=) p.(=)