Product Details

SNP ID

rs752758

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.9:113360207 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTGACCTTGTATTCCCAACTGTGAT[A/T]AAGCAGAGTATTCTAGTTGGGCTCT

Phenotype

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

BSPRY PubMed Links

Additional Information

For this assay, SNP(s) [rs79435708] 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

BSPRY

Gene Name

B-box and SPRY domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317943.1		Intron			NP_001304872.1
NM_001317944.1		Intron			NP_001304873.1
NM_017688.2		Intron			NP_060158.2
XM_006717149.3		Intron			XP_006717212.1

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