Product Details

SNP ID

rs9556851

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:97953659 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGACGTCTCTGAGCCAGGAGGTCA[A/G]AACTGTGGGATTGATGACCTCCCAC

Phenotype

MIM: 602008

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

IPO5 PubMed Links

Additional Information

For this assay, SNP(s) [rs79312465] 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

IPO5

Gene Name

importin 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002271.4	19	Intron			NP_002262.3
XM_005254052.3	19	Intron			XP_005254109.1
XM_005254053.3	19	Intron			XP_005254110.1
XM_011521087.2	19	UTR 5			XP_011519389.1
XM_011521088.2	19	UTR 5			XP_011519390.1
XM_011521089.2	19	UTR 5			XP_011519391.1
XM_011521090.2	19	Intron			XP_011519392.1
XM_017020562.1	19	UTR 5			XP_016876051.1

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