Product Details

SNP ID

rs2301363

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.9:137139979 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GCCACCTTGGCTGGTCCTCAGAGGG[T/C]CCCTGGGGCTCCAGGCCCTGACTGG

Phenotype

MIM: 138249

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

GRIN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs76135674] 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

GRIN1

Gene Name

glutamate ionotropic receptor NMDA type subunit 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000832.6		Intron			NP_000823.4
NM_001185090.1		Intron			NP_001172019.1
NM_001185091.1		Intron			NP_001172020.1
NM_007327.3		Intron			NP_015566.1
NM_021569.3		Intron			NP_067544.1
XM_005266071.3		Intron			XP_005266128.1
XM_005266072.3		Intron			XP_005266129.1
XM_005266073.4		Intron			XP_005266130.1
XM_011518583.2		Intron			XP_011516885.1

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