Product Details

SNP ID

rs7819231

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:117523159 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTTCAAAAAAAGTATTTTATCAA[A/T]AACTAGATTACATGTGGACCTGCAT

Phenotype

MIM: 610237

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

MED30 PubMed Links

Additional Information

For this assay, SNP(s) [rs202104794] 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

MED30

Gene Name

mediator complex subunit 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282986.1		Intron			NP_001269915.1
NM_080651.3		Intron			NP_542382.1
XM_011517360.2		Intron			XP_011515662.1

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