Product Details

SNP ID

rs7133066

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:116922812 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACCCCTTTGAGTGTGTGTGTGTGT[G/T]TTTTTTTTCCCTTGACTAGGAAAAA

Phenotype

MIM: 609073

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

FBXW8 PubMed Links

Additional Information

For this assay, SNP(s) [rs185670083] 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

FBXW8

Gene Name

F-box and WD repeat domain containing 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012174.1		Intron			NP_036306.1
NM_153348.2		Intron			NP_699179.2
XM_005253867.2		Intron			XP_005253924.1
XM_005253868.3		Intron			XP_005253925.1
XM_017019175.1		Intron			XP_016874664.1
XM_017019176.1		Intron			XP_016874665.1
XM_017019177.1		Intron			XP_016874666.1
XM_017019178.1		Intron			XP_016874667.1

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