Product Details

SNP ID
rs200297262
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:87305901 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGCCAGCAGCATGCATCCAGCAG[G/T]GGTGCTAGGCAAAGAAAAGGTGGGT
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
C16orf95 PubMed Links

Gene Details

Gene
C16orf95
Gene Name
chromosome 16 open reading frame 95
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195124.1 517 Silent Mutation CCA,CCC P173P NP_001182053.1
NM_001195125.1 517 Missense Mutation CAC,CCC H112P NP_001182054.1
NM_001256917.1 517 Missense Mutation CAC,CCC H97P NP_001243846.1

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