Product Details

SNP ID

rs17154147

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:80602690 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTCAGAAAACCCAAACTTCTCGTG[A/G]CTTCAAAAAGTGTAATTGTACCTGA

Phenotype

MIM: 173510

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CD36 PubMed Links

Additional Information

For this assay, SNP(s) [rs1880410] 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

CD36

Gene Name

CD36 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000072.3		Intron			NP_000063.2
NM_001001547.2		Intron			NP_001001547.1
NM_001001548.2		Intron			NP_001001548.1
NM_001127443.1		Intron			NP_001120915.1
NM_001127444.1		Intron			NP_001120916.1
NM_001289908.1		Intron			NP_001276837.1
NM_001289909.1		Intron			NP_001276838.1
NM_001289911.1		Intron			NP_001276840.1
XM_005250713.1		Intron			XP_005250770.1
XM_005250714.1		Intron			XP_005250771.1
XM_005250715.4		Intron			XP_005250772.1

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