Product Details

SNP ID

rs28676928

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:20515222 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCATGCTATGCCAAGCCCTGTTGC[A/T]GGAGTTGACAGATGTTGACTCATCC

Phenotype

MIM: 607372

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

MED15 PubMed Links

Additional Information

For this assay, SNP(s) [rs116522857] 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

MED15

Gene Name

mediator complex subunit 15

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003891.2		Intron			NP_001003891.1
NM_001293234.1		Intron			NP_001280163.1
NM_001293235.1		Intron			NP_001280164.1
NM_001293236.1		Intron			NP_001280165.1
NM_001293237.1		Intron			NP_001280166.1
NM_015889.4		Intron			NP_056973.2
XM_006724263.3		Intron			XP_006724326.1
XM_006724264.3		Intron			XP_006724327.1
XM_011530214.2		Intron			XP_011528516.1
XM_011530215.2		Intron			XP_011528517.1
XM_011530218.2		Intron			XP_011528520.1
XM_011530219.1		Intron			XP_011528521.1
XM_011530220.2		Intron			XP_011528522.1
XM_017028817.1		Intron			XP_016884306.1
XM_017028818.1		Intron			XP_016884307.1
XM_017028819.1		Intron			XP_016884308.1
XM_017028820.1		Intron			XP_016884309.1
XM_017028821.1		Intron			XP_016884310.1
XM_017028822.1		Intron			XP_016884311.1
XM_017028823.1		Intron			XP_016884312.1
XM_017028824.1		Intron			XP_016884313.1

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