Product Details

SNP ID

rs202058619

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:94115876 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCATAGCAGCCAAGATGATGTCC[A/G]CGGCGGCCATTGCCAATGGGGGTGG

Phenotype

MIM: 600009

Polymorphism

A/G, 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	396	Missense Mutation	ACG,GCG	T73A	NP_001123552.1
NM_001288952.1	396	Missense Mutation	ACG,GCG	T73A	NP_001275881.1
NM_001288954.1	396	Missense Mutation	ACG,GCG	T70A	NP_001275883.1
NM_001288956.1	396	Missense Mutation	ACG,GCG	T73A	NP_001275885.1
NM_001288957.1	396	Missense Mutation	ACG,GCG	T70A	NP_001275886.1
NM_001288958.1	396	Missense Mutation	ACG,GCG	T70A	NP_001275887.1
NM_001288959.1	396	Missense Mutation	ACG,GCG	T30A	NP_001275888.1
NM_001288960.1	396	Missense Mutation	ACG,GCG	T25A	NP_001275889.1
NM_001288995.1	396	Missense Mutation	ACG,GCG	T70A	NP_001275924.1
NM_005532.4	396	Missense Mutation	ACG,GCG	T70A	NP_005523.3

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