Variant #0000000112 (NC_000016.9:g.50733539G>A, NM_022162.1:c.214G>A (NOD2))

Chromosome 16
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.50733539G>A
Reference -
DB-ID NOD2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner Sabine Heber
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Sabine Heber
Date created 2020-10-08 11:20:03 +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 +?/+? 2 c.214G>A r.(?) p.(Glu72Lys)