Product Details

SNP ID

rs201333197

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15615750 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGACCTATGCCTTCTATCACAACG[G/T]CCGCCGCCTCCGGTGTTTCCCGCAG

Phenotype

MIM: 611545

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CYP4F8 PubMed Links

Additional Information

For this assay, SNP(s) [rs73001907] 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

CYP4F8

Gene Name

cytochrome P450 family 4 subfamily F member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007253.3	135	Missense Mutation	GGC,GTC	G45V	NP_009184.1
XM_017026232.1	135	Missense Mutation	GGC,GTC	G45V	XP_016881721.1

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