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SNP ID: rs151265454
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:1010433 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCTACCGCAGCCCCCAGGGGAGTTG[C/T]GTCAGAAGCTGCGGAGTCACTCGGG
Phenotype: MIM: 606651 MIM: 611011
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GRIN3B PubMed Links

Gene Details

Gene: GRIN3B
Gene Name: glutamate ionotropic receptor NMDA type subunit 3B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138690.2	2025	Intron			NP_619635.1
XM_017026243.1	2025	Intron			XP_016881732.1

Gene: LOC105372235
Gene Name: uncharacterized LOC105372235

There are no transcripts associated with this gene.

Gene: TMEM259
Gene Name: transmembrane protein 259

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033026.1	2025	Missense Mutation	ACA,GCA	T594A	NP_001028198.1
NM_033420.3	2025	UTR 3			NP_219488.1
XM_005259675.2	2025	Missense Mutation	ACA,GCA	T635A	XP_005259732.1
XM_005259676.2	2025	Missense Mutation	ACA,GCA	T629A	XP_005259733.1
XM_005259677.2	2025	Missense Mutation	ACA,GCA	T618A	XP_005259734.1
XM_005259678.2	2025	Missense Mutation	ACA,GCA	T600A	XP_005259735.1
XM_017027457.1	2025	Missense Mutation	ACA,GCA	T583A	XP_016882946.1

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