Product Details

SNP ID

rs2713935

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56254014 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACATAGGTTATCACCCACAAATTA[C/T]ATTTAATGGTGTTTTGAAAGAGTTA

Phenotype

MIM: 612660

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RFX7 PubMed Links

Additional Information

For this assay, SNP(s) [rs115786351] 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

RFX7

Gene Name

regulatory factor X7

There are no transcripts associated with this gene.

Gene

TEX9

Gene Name

testis expressed 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286449.1		Intron			NP_001273378.1
NM_198524.2		Intron			NP_940926.1
XM_005254359.4		Intron			XP_005254416.1
XM_005254361.3		Intron			XP_005254418.1
XM_011521530.2		Intron			XP_011519832.1
XM_017022160.1		Intron			XP_016877649.1
XM_017022161.1		Intron			XP_016877650.1
XM_017022162.1		Intron			XP_016877651.1
XM_017022163.1		Intron			XP_016877652.1
XM_017022164.1		Intron			XP_016877653.1
XM_017022166.1		Intron			XP_016877655.1
XM_017022167.1		Intron			XP_016877656.1

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