Product Details

SNP ID

rs10827888

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:19825350 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTATGGAAAAACTGCATAGGAATCC[A/G]AATATTTGAAAGTCAATTCTCTATG

Phenotype

MIM: 606827

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PLXDC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs117654818] 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

PLXDC2

Gene Name

plexin domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282736.1		Intron			NP_001269665.1
NM_032812.8		Intron			NP_116201.7
XM_011519750.2		Intron			XP_011518052.1

View Full Product Details