Product Details

SNP ID

rs3848540

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:48448310 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTGATCAGGTAGACTTGTAAGTA[A/C]AATGATACGGTATATGAAGAGCACT

Phenotype

MIM: 602717 MIM: 610597 MIM: 603953

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

GRIN2D PubMed Links

Additional Information

For this assay, SNP(s) [rs77344668] 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

GRIN2D

Gene Name

glutamate ionotropic receptor NMDA type subunit 2D

There are no transcripts associated with this gene.

Gene

GRWD1

Gene Name

glutamate rich WD repeat containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031485.3		Intron			NP_113673.3

Gene

KCNJ14

Gene Name

potassium voltage-gated channel subfamily J member 14

There are no transcripts associated with this gene.

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