Product Details

SNP ID

rs4941624

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:48078251 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAACTAGAAAGGTATGCCAGTTAGC[C/T]TCAAATCTACCCTTCTCTCTGGCCC

Phenotype

MIM: 605718

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MED4 PubMed Links

Additional Information

For this assay, SNP(s) [rs143736630] 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

MED4

Gene Name

mediator complex subunit 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270629.1		Intron			NP_001257558.1
NM_014166.3		Intron			NP_054885.1
XM_017020549.1		Intron			XP_016876038.1

Gene

MED4-AS1

Gene Name

MED4 antisense RNA 1

There are no transcripts associated with this gene.

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