Product Details

SNP ID

rs111889356

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:95405465 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTAGTCACTGTAGGCTTCTCAGA[C/T]AGAATGTTCTGGATGCGGAGAACCT

Phenotype

MIM: 602447 MIM: 602720

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PON2 PubMed Links

Additional Information

For this assay, SNP(s) [rs7493] 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

PON2

Gene Name

paraoxonase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000305.2	926	Silent Mutation	CTA,CTG	L310L	NP_000296.2
NM_001018161.1	926	Silent Mutation	CTA,CTG	L298L	NP_001018171.1
XM_005250453.1	926	Silent Mutation	CTA,CTG	L242L	XP_005250510.1
XM_017012357.1	926	Silent Mutation	CTA,CTG	L240L	XP_016867846.1
XM_017012358.1	926	Silent Mutation	CTA,CTG	L224L	XP_016867847.1

Gene

PON3

Gene Name

paraoxonase 3

There are no transcripts associated with this gene.

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