Product Details

SNP ID
rs200270667
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:27067006 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGCCCCCTCTCCCTGGATAAAC[C/T]ACTTCAGCTGCCCCCCATTTTTCTC
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_001145545.1 109 Missense Mutation CCA,CTA P4L NP_001139017.1

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