Product Details

SNP ID

rs7794625

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:5459264 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CACAGGTCTGCAGAGATGGACCACA[A/G]GGCCCTGGCCTTGGCTCAGCCCCAG

Phenotype

MIM: 609084

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FBXL18 PubMed Links

Additional Information

For this assay, SNP(s) [rs114414141] 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

FBXL18

Gene Name

F-box and leucine rich repeat protein 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321213.1		Intron			NP_001308142.1
NM_024963.5		Intron			NP_079239.3
XM_011515531.2		Intron			XP_011513833.1
XM_011515532.2		Intron			XP_011513834.1

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