Product Details

SNP ID

rs9584732

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:97966383 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAAAAGCTTATCCTGCATCAATTG[A/C]GATGCTCATATAGTTTTTACGCTTT

Phenotype

MIM: 602008

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

IPO5 PubMed Links

Additional Information

For this assay, SNP(s) [rs78039536] 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		Intron			NP_002262.3
XM_005254052.3		Intron			XP_005254109.1
XM_005254053.3		Intron			XP_005254110.1
XM_011521087.2		Intron			XP_011519389.1
XM_011521088.2		Intron			XP_011519390.1
XM_011521089.2		Intron			XP_011519391.1
XM_011521090.2		Intron			XP_011519392.1
XM_017020562.1		Intron			XP_016876051.1

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