Variant #0000000160 (NC_000016.9:g.50756540G>C, NM_022162.1:c.2722G>C (NOD2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.50756540G>C
Reference -
DB-ID NOD2_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 0.01126 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 09:02:12 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOD2 NM_022162.1 +/+ 88 c.2722G>C r.(?) p.(Gly908Arg)