Product Details

SNP ID

rs4252079

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:160710914 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGAATACATGAATCAAAGAATGG[C/T]TCAGTTTACTGCAGCCTTTTTGCAG

Phenotype

MIM: 173350

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLG PubMed Links

Additional Information

For this assay, SNP(s) [rs4252080] 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

PLG

Gene Name

plasminogen

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000301.3		Intron			NP_000292.1
NM_001168338.1		Intron			NP_001161810.1

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