Product Details

SNP ID

rs1533591

Assay Type

Functionally Tested

NCBI dbSNP Submissions

47

Location

Chr.1:224115976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTAGAGTTAAAACACATCCCACAA[C/T]TTATGAATAAATGACATCTCTGTCA

Phenotype

MIM: 609100

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FBXO28 PubMed Links

Additional Information

For this assay, SNP(s) [rs114786314] are located under a probe 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

FBXO28

Gene Name

F-box protein 28

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136115.2		Intron			NP_001129587.1
NM_015176.3		Intron			NP_055991.1

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