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SNP ID

rs117088942

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:56361868 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTGTAGCATTCACACCACCCTGG[C/T]GGTAGAGCTGTAGCTGTAGAGCCCA

Phenotype

MIM: 107760 MIM: 600556

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

APOF PubMed Links

Gene Details

Gene

APOF

Gene Name

apolipoprotein F

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001638.2	392	Missense Mutation	CAC,CGC	H113R	NP_001629.1

Gene

STAT2

Gene Name

signal transducer and activator of transcription 2

There are no transcripts associated with this gene.

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