Product Details

SNP ID

rs3969069

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:51287236 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGATCGTAGCATACTACAGTGTC[A/G]AACACCTGGGCTCAAGTGATCCTCC

Phenotype

MIM: 605936

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

BIN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs545131325] are located under a probe 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

BIN2

Gene Name

bridging integrator 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001290007.1		Intron			NP_001276936.1
NM_001290008.1		Intron			NP_001276937.1
NM_001290009.1		Intron			NP_001276938.1
NM_016293.3		Intron			NP_057377.3
XM_005268957.3		Intron			XP_005269014.2
XM_005268958.3		Intron			XP_005269015.1
XM_017019422.1		Intron			XP_016874911.1

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