Product Details

SNP ID

rs11753888

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:46796226 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGGGGCTCATCAACGGGTGTTGAC[C/T]AAGCCTTCCAAGGGACTCTGATGCT

Phenotype

MIM: 600388

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MEP1A PubMed Links

Additional Information

For this assay, SNP(s) [rs111532700] 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

MEP1A

Gene Name

meprin A subunit alpha

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005588.2		Intron			NP_005579.2
XM_011514628.1		Intron			XP_011512930.1
XM_011514629.1		Intron			XP_011512931.1

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