Product Details

SNP ID

rs56211739

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:171862109 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAAAAAATCCATTCATTCATTCAG[A/G]ATTGCCTCCTCCCCTGCCCCCTCCC

Phenotype

MIM: 605651

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FBXW11 PubMed Links

Additional Information

For this assay, SNP(s) [rs61028744] 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

FBXW11

Gene Name

F-box and WD repeat domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012300.2	3576	UTR 3			NP_036432.2
NM_033644.2	3576	UTR 3			NP_387448.2
NM_033645.2	3576	UTR 3			NP_387449.2
XM_005265855.4	3576	UTR 3			XP_005265912.1
XM_005265856.2	3576	UTR 3			XP_005265913.1
XM_005265857.2	3576	UTR 3			XP_005265914.1
XM_005265858.2	3576	UTR 3			XP_005265915.1
XM_017009279.1	3576	UTR 3			XP_016864768.1
XM_017009280.1	3576	UTR 3			XP_016864769.1
XM_017009281.1	3576	UTR 3			XP_016864770.1

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