Variant #0000967647 (NC_000010.10:g.3827248G>C, NM_001160124.1:c.-42C>G (KLF6))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.3827248G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KLF6_000054
Frequency 2/12966
Freq. EA 0/8580
Freq. AA 2/4386
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 18:42:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KLF6 NM_001160124.1 ?/? c.-42C>G r.(=) p.(=)