Product Details

SNP ID

rs10484565

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:32827255 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAGTCCCTCCCAACAACCAGTGAT[A/G]TGTACAATGTTGCATTTTCAGTGGT

Phenotype

MIM: 170261

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TAP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs17213777,rs17220185] 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

TAP2

Gene Name

transporter 2, ATP binding cassette subfamily B member

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000544.3	3887	UTR 3			NP_000535.3
NM_001290043.1	3887	UTR 3			NP_001276972.1
NM_018833.2	3887	Intron			NP_061313.2

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