Product Details

SNP ID
rs77619135
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:92304743 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGAATGCGGATTCGATCATTCACAT[C/T]GGTAAGAAAGTGTTGGTGCAGCTCG
Phenotype
MIM: 602368
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GRID2 PubMed Links

Gene Details

Gene
GRID2
Gene Name
glutamate ionotropic receptor delta type subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286838.1 495 Silent Mutation ATC,ATT I29I NP_001273767.1
NM_001510.3 495 Silent Mutation ATC,ATT I29I NP_001501.2
XM_011531893.2 495 Intron XP_011530195.2
XM_011531894.2 495 Intron XP_011530196.1
XM_011531895.2 495 Intron XP_011530197.1
XM_017008118.1 495 Intron XP_016863607.1
XM_017008119.1 495 Intron XP_016863608.1
XM_017008120.1 495 Intron XP_016863609.1
XM_017008121.1 495 Intron XP_016863610.1
XM_017008122.1 495 Silent Mutation ATC,ATT I29I XP_016863611.1
XM_017008123.1 495 Intron XP_016863612.1
XM_017008124.1 495 Intron XP_016863613.1
XM_017008125.1 495 Intron XP_016863614.1
XM_017008126.1 495 Intron XP_016863615.1
XM_017008127.1 495 Intron XP_016863616.1

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