Product Details

SNP ID

rs199546813

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:46394482 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCGGGGCGCGGTGGTCCGGGCGC[A/G]ACAGAGGCAGCGAGCGGGCCTGGAG

Phenotype

MIM: 602935

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAAH PubMed Links

Gene Details

Gene

FAAH

Gene Name

fatty acid amide hydrolase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001441.2	216	Missense Mutation	CAA,CGA	Q45R	NP_001432.2

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