View genomic variant #0000000112

Chromosome 16
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.50733539G>A
Reference -
DB-ID NOD2_000001
Frequency -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Sabine Heber




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)