Product Details

SNP ID

rs10412841

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51798318 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTTGCTACTGGCATCTCTGGATAG[A/C]GGCCAGGGGTGCCGCTAAACATCCT

Phenotype

MIM: 136539

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FPR3 PubMed Links

Additional Information

For this assay, SNP(s) [rs115181030] 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

FPR3

Gene Name

formyl peptide receptor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002030.4		Intron			NP_002021.3
XM_011526687.2		Intron			XP_011524989.1

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