Product Details

SNP ID

rs4848980

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.2:112058771 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATTGCAGAAATTAGGCAGGAAATGC[A/G]GAGGGCCTAAATTAGGGCAGTGGTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TMEM87B PubMed Links

Additional Information

For this assay, SNP(s) [rs116046835,rs72940089] 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

TMEM87B

Gene Name

transmembrane protein 87B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032824.2		Intron			NP_116213.1
XM_005263827.2		Intron			XP_005263884.1
XM_006712807.2		Intron			XP_006712870.1
XM_017005121.1		Intron			XP_016860610.1

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