Product Details

SNP ID

rs7662929

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:75912935 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TACGACACTGTCCAAGAAGAAACAC[A/G]AATATTCTGGGCCACTAGAGACGTC

Phenotype

MIM: 607469

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NAAA PubMed Links

Additional Information

For this assay, SNP(s) [rs144233384] are located under a primer 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

NAAA

Gene Name

N-acylethanolamine acid amidase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042402.1		Intron			NP_001035861.1
NM_014435.3		Intron			NP_055250.2
XM_005262920.3		Intron			XP_005262977.1
XM_005262921.3		Intron			XP_005262978.1
XM_005262923.2		Intron			XP_005262980.1
XM_005262924.2		Intron			XP_005262981.1
XM_005262925.3		Intron			XP_005262982.1
XM_006714180.2		Intron			XP_006714243.1
XM_011531852.2		Intron			XP_011530154.1
XM_011531854.2		Intron			XP_011530156.1
XM_017008027.1		Intron			XP_016863516.1
XM_017008028.1		Intron			XP_016863517.1
XM_017008029.1		Intron			XP_016863518.1
XM_017008030.1		Intron			XP_016863519.1

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