Product Details

SNP ID
rs202049406
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:94115875 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCCATAGCAGCCAAGATGATGTC[C/T]GCGGCGGCCATTGCCAATGGGGGTG
Phenotype
MIM: 600009
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
IFI27 PubMed Links

Gene Details

Gene
IFI27
Gene Name
interferon alpha inducible protein 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130080.2 395 Silent Mutation TCC,TCT S72S NP_001123552.1
NM_001288952.1 395 Silent Mutation TCC,TCT S72S NP_001275881.1
NM_001288954.1 395 Silent Mutation TCC,TCT S69S NP_001275883.1
NM_001288956.1 395 Silent Mutation TCC,TCT S72S NP_001275885.1
NM_001288957.1 395 Silent Mutation TCC,TCT S69S NP_001275886.1
NM_001288958.1 395 Silent Mutation TCC,TCT S69S NP_001275887.1
NM_001288959.1 395 Silent Mutation TCC,TCT S29S NP_001275888.1
NM_001288960.1 395 Silent Mutation TCC,TCT S24S NP_001275889.1
NM_001288995.1 395 Silent Mutation TCC,TCT S69S NP_001275924.1
NM_005532.4 395 Silent Mutation TCC,TCT S69S NP_005523.3

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