Product Details

SNP ID

rs12334564

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:123768584 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TAGGCCATGGGGCAGCCTGGGCCTT[A/C]TGCAGTGTGAGGCGCGGGGCCTCCC

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FAM91A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs142309473] are located under a probe 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

FAM91A1

Gene Name

family with sequence similarity 91 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317917.1	146	UTR 5			NP_001304846.1
NM_001317918.1	146	UTR 5			NP_001304847.1
NM_144963.3	146	UTR 5			NP_659400.2

View Full Product Details