Product Details

SNP ID

rs144789024

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:19116596 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGACAGGAGGGTGTGGCACGTGGT[C/T]TGGAGCTGCTGAGTCAGGTTGCGGG

Phenotype

MIM: 103195

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLIN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2229536] 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

PLIN2

Gene Name

perilipin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122.3	988	Intron			NP_001113.2
XM_017014259.1	988	Missense Mutation			XP_016869748.1

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