Product Details

SNP ID

rs10985027

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:120759885 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCAAAACAGCTTTTTGCACTGAGC[A/G]TGACCATTCAGTCTGATTAGGCTGA

Phenotype

MIM: 609071

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FBXW2 PubMed Links

Additional Information

For this assay, SNP(s) [rs138480685] 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

FBXW2

Gene Name

F-box and WD repeat domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012164.3	6085	UTR 3			NP_036296.2
XM_005251910.3	6085	UTR 3			XP_005251967.1
XM_005251913.2	6085	UTR 3			XP_005251970.1
XM_006717049.3	6085	UTR 3			XP_006717112.1
XM_006717051.2	6085	UTR 3			XP_006717114.1
XM_011518518.1	6085	UTR 3			XP_011516820.1
XM_017014615.1	6085	UTR 3			XP_016870104.1
XM_017014616.1	6085	UTR 3			XP_016870105.1
XM_017014617.1	6085	UTR 3			XP_016870106.1

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