Variant #0001546384 (NC_000017.10:g.6659490T>C, NC_000017.10(NM_017523.2):c.32+61T>C (XAF1))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.6659490T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID XAF1_000014
Frequency 59/4566
Freq. EA 0/3182
Freq. AA 59/1384
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 15:52:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
XAF1 NM_017523.2 ?/? c.32+61T>C r.(=) p.(=)