Product Details

SNP ID

rs2566119

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:39053023 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGCTGAAGTTAAATTATTGAACAG[G/T]TTATTGGTGGCTTTTCTTTGGGTCT

Phenotype

MIM: 608064

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

KLHL5 PubMed Links

Additional Information

For this assay, SNP(s) [rs78681578] 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

KLHL5

Gene Name

kelch like family member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007075.2		Intron			NP_001007076.1
NM_001171654.1		Intron			NP_001165125.1
NM_015990.4		Intron			NP_057074.3
NM_199039.3		Intron			NP_950240.2
XM_005262655.4		Intron			XP_005262712.1
XM_011513699.2		Intron			XP_011512001.1
XM_011513700.2		Intron			XP_011512002.1
XM_011513701.2		Intron			XP_011512003.1
XM_017008273.1		Intron			XP_016863762.1
XM_017008274.1		Intron			XP_016863763.1
XM_017008275.1		Intron			XP_016863764.1
XM_017008276.1		Intron			XP_016863765.1

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