Product Details

SNP ID

rs149698079

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:74716465 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGGGTCATGTCATAGAGGACGTA[A/G]CCCAGGAGGCCCCCCGCAAACACAG

Phenotype

MIM: 611026

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FA2H PubMed Links

Additional Information

For this assay, SNP(s) [rs11554620] 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

FA2H

Gene Name

fatty acid 2-hydroxylase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024306.4	696	Silent Mutation	GGC,GGT	G307G	NP_077282.3
XM_011523317.2	696	UTR 3			XP_011521619.1
XM_011523319.2	696	Silent Mutation	GGC,GGT	G227G	XP_011521621.1

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