Product Details

SNP ID

rs140643844

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:94115843 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGGGCTTCACTGCGGCGGGAATC[A/G]CCTCGTCCTCCATAGCAGCCAAGAT

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	363	Missense Mutation	ACC,GCC	T62A	NP_001123552.1
NM_001288952.1	363	Missense Mutation	ACC,GCC	T62A	NP_001275881.1
NM_001288954.1	363	Missense Mutation	ACC,GCC	T59A	NP_001275883.1
NM_001288956.1	363	Missense Mutation	ACC,GCC	T62A	NP_001275885.1
NM_001288957.1	363	Missense Mutation	ACC,GCC	T59A	NP_001275886.1
NM_001288958.1	363	Missense Mutation	ACC,GCC	T59A	NP_001275887.1
NM_001288959.1	363	Missense Mutation	ACC,GCC	T19A	NP_001275888.1
NM_001288960.1	363	Missense Mutation	ACC,GCC	T14A	NP_001275889.1
NM_001288995.1	363	Missense Mutation	ACC,GCC	T59A	NP_001275924.1
NM_005532.4	363	Missense Mutation	ACC,GCC	T59A	NP_005523.3

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