Product Details

SNP ID

rs13270979

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:66668462 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGATTTTTACGCTGCTGCTTACC[A/T]AAAAATCCCGGCCGGGCGCGGTGGC

Phenotype

MIM: 611745

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

C8orf44 PubMed Links

Additional Information

For this assay, SNP(s) [rs143635222] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

C8orf44

Gene Name

chromosome 8 open reading frame 44

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019607.2		Intron			NP_062553.1

Gene

C8orf44-SGK3

Gene Name

C8orf44-SGK3 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204173.1		Intron			NP_001191102.1

Gene

VCPIP1

Gene Name

valosin containing protein interacting protein 1

There are no transcripts associated with this gene.

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