Product Details

SNP ID

rs77520296

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:48404830 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGGAGTATGACTGGACGTCCTTT[G/T]TAGCCGTGACCACTCGTGCCCCTGG

Phenotype

MIM: 602717

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

GRIN2D PubMed Links

Gene Details

Gene

GRIN2D

Gene Name

glutamate ionotropic receptor NMDA type subunit 2D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000836.2	650	Missense Mutation	GTA,TTA	V188L	NP_000827.2
XM_011526872.1	650	Missense Mutation	GTA,TTA	V188L	XP_011525174.1

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