Product Details

SNP ID
rs114324679
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:27067141 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCGTGGCCACGCCATGCAGGAG[C/T]GGCTCAGGAGCCCCTGAAAGTGTCC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C16orf82 PubMed Links

Gene Details

Gene
C16orf82
Gene Name
chromosome 16 open reading frame 82
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145545.1 244 Missense Mutation GCG,GTG A49V NP_001139017.1

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