Variant #0000320078 (NC_000002.11:g.220078960G>A, NC_000002.11(NM_005689.2):c.1387-52C>T (ABCB6))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.220078960G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCB6_000112
Frequency 1/7272
Freq. EA 1/4618
Freq. AA 0/2654
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 16:22:05 +02:00 (CEST)
Date last edited 2025-01-04 19:57:50 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 ?/? c.1387-52C>T r.(=) p.(=)