Product Details

SNP ID

rs12280272

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:129380511 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCAGTCAGAGACCCAAACTCATAG[A/G]ATCTTAGGAACCTGAGAGTTGGATA

Phenotype

MIM: 604823

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

BARX2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115776058] 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

BARX2

Gene Name

BARX homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003658.4		Intron			NP_003649.2
XM_011543043.1		Intron			XP_011541345.1
XM_011543044.2		Intron			XP_011541346.1

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