Product Details

SNP ID

rs143911724

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:93566914 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCAACGTGTGCGCCCTGGTGCTGG[C/T]GGCGCGCCGACGACGCCGCGGCGCG

Phenotype

MIM: 609044

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FFAR4 PubMed Links

Additional Information

For this assay, SNP(s) [rs61866610] 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

FFAR4

Gene Name

free fatty acid receptor 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195755.1	736	Missense Mutation	GCG,GTG	A65V	NP_001182684.1
NM_181745.3	736	Missense Mutation	GCG,GTG	A65V	NP_859529.2
XM_011539746.2	736	Missense Mutation	GCG,GTG	A65V	XP_011538048.1

View Full Product Details