Variant #0000000312 (NC_000002.11:g.10188123C>T, NM_003597.4:c.659C>T (KLF11))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.10188123C>T
Reference -
DB-ID KLF11_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00323 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-17 12:10:07 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLF11 NM_003597.4 +/+ - c.659C>T r.(?) p.(Thr220Met)