Product Details

SNP ID

rs17488436

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:165259865 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTCGCTGTATGACTTGGTCAAGCC[A/G]TTTAACCCCTCGAGGGTGTGGTTTC

Phenotype

MIM: 605774

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

KLHL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs200290411] 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

KLHL2

Gene Name

kelch like family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161521.1		Intron			NP_001154993.1
NM_001161522.1		Intron			NP_001154994.1
NM_007246.3		Intron			NP_009177.3
XM_011531572.2		Intron			XP_011529874.1
XM_011531575.2		Intron			XP_011529877.1
XM_011531576.2		Intron			XP_011529878.1
XM_017007674.1		Intron			XP_016863163.1
XM_017007675.1		Intron			XP_016863164.1
XM_017007676.1		Intron			XP_016863165.1
XM_017007677.1		Intron			XP_016863166.1

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