Product Details

SNP ID

rs28362586

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:2793747 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAAAGCCGCCCACTGGCGCTGATT[C/G]ACACTGAAGTGTGAGTGACTGATAG

Phenotype

MIM: 602104

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SH3BP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs112076089] 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

SH3BP2

Gene Name

SH3 domain binding protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122681.1		Intron			NP_001116153.1
NM_001145855.1		Intron			NP_001139327.1
NM_001145856.1		Intron			NP_001139328.1
NM_003023.4		Intron			NP_003014.3

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