Product Details

SNP ID

rs16939668

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:85778658 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAAATAAAGCACATTTATTGTAGC[A/G]ATGTCTGAACTTTTTTCCTATGTGT

Phenotype

MIM: 604886

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

EMC8 PubMed Links

Additional Information

For this assay, SNP(s) [rs77962984] 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

EMC8

Gene Name

ER membrane protein complex subunit 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142288.1	1621	UTR 3			NP_001135760.1
NM_006067.4	1621	UTR 3			NP_006058.1
XM_011522813.2	1621	Intron			XP_011521115.1
XM_017022867.1	1621	UTR 3			XP_016878356.1

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