Product Details

SNP ID

rs13250483

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:95248498 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTTTCTGATGAATTAACTATAGAA[A/T]ATTTTCATTAGCTTCAATGATCTGT

Phenotype

MIM: 614477

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

C8orf37 PubMed Links

Additional Information

For this assay, SNP(s) [rs80034424] 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

C8orf37

Gene Name

chromosome 8 open reading frame 37

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_177965.3		Intron			NP_808880.1
XM_005250799.3		Intron			XP_005250856.2

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