Product Details

SNP ID

rs10476016

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:172328091 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTTTGTAATTTTTATAGACATGG[A/G]ATCTCGCTACGTTGCCTAGTAGGCT

Phenotype

MIM: 613293

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SH3PXD2B PubMed Links

Additional Information

For this assay, SNP(s) [rs140184137] 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

SH3PXD2B

Gene Name

SH3 and PX domains 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017995.2		Intron			NP_001017995.1
NM_001308175.1		Intron			NP_001295104.1
XM_017009351.1		Intron			XP_016864840.1

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