Variant #0000695375 (NC_000006.11:g.136597667G>C, NC_000006.11(NM_014739.2):c.1017-21C>G (BCLAF1))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.136597667G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCLAF1_000099
Frequency 5/12990
Freq. EA 5/8592
Freq. AA 0/4398
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 16:27:59 +02:00 (CEST)
Date last edited 2013-05-04 10:43:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCLAF1 NM_014739.2 ?/? c.1017-21C>G r.(=) p.(=)