Product Details

SNP ID

rs16923193

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:5512459 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCTGCTTTGAGGGATTTTCCTCCA[C/T]TGCCTCAGAAGTACTGCCCTGGGGG

Phenotype

MIM: 605723

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PDCD1LG2 PubMed Links

Additional Information

For this assay, SNP(s) [rs57093377] 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

PDCD1LG2

Gene Name

programmed cell death 1 ligand 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025239.3		Intron			NP_079515.2
XM_005251600.3		Intron			XP_005251657.1

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