Product Details

SNP ID

rs201359065

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:68155375 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATTACTGGGATGCTCTTCGACCT[C/T]GAAACAGCATCTGACTCCTTTTTCG

Phenotype

MIM: 147570

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

IFNG PubMed Links

Gene Details

Gene

IFNG

Gene Name

interferon gamma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000619.2	605	Missense Mutation	CAA,CGA	Q160R	NP_000610.2

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