Product Details

SNP ID
rs201422008
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:24240146 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTAATGACGGAGCTGCACAGAGAC[A/G]GAGGACACACTGTAGGAGGGAAACC
Phenotype
MIM: 610781 MIM: 603171 MIM: 190195 MIM: 604319
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
GMPR2 PubMed Links
Additional Information
For this assay, SNP(s) [rs10141326] are located under a probe 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
GMPR2
Gene Name
guanosine monophosphate reductase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001002000.2 1013 Intron NP_001002000.1
NM_001002001.2 1013 Intron NP_001002001.1
NM_001002002.2 1013 Intron NP_001002002.1
NM_001283021.1 1013 Intron NP_001269950.1
NM_001283022.1 1013 Intron NP_001269951.1
NM_001283023.1 1013 Intron NP_001269952.1
NM_016576.4 1013 Intron NP_057660.2
XM_005267740.3 1013 Intron XP_005267797.1
XM_005267741.3 1013 Intron XP_005267798.1
XM_005267742.3 1013 Intron XP_005267799.1
XM_006720165.2 1013 Intron XP_006720228.1
XM_017021356.1 1013 Intron XP_016876845.1
XM_017021357.1 1013 Intron XP_016876846.1
XM_017021358.1 1013 Intron XP_016876847.1
XM_017021359.1 1013 Intron XP_016876848.1
XM_017021360.1 1013 Intron XP_016876849.1
Gene
NEDD8
Gene Name
neural precursor cell expressed, developmentally down-regulated 8
There are no transcripts associated with this gene.

Gene
NEDD8-MDP1
Gene Name
NEDD8-MDP1 readthrough
There are no transcripts associated with this gene.

Gene
TGM1
Gene Name
transglutaminase 1
There are no transcripts associated with this gene.

Gene
TINF2
Gene Name
TERF1 interacting nuclear factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099274.1 1013 Missense Mutation NP_001092744.1
NM_012461.2 1013 UTR 3 NP_036593.2
XM_005267529.3 1013 Missense Mutation XP_005267586.1
XM_011536642.2 1013 UTR 3 XP_011534944.1
XM_017021216.1 1013 Missense Mutation XP_016876705.1
XM_017021217.1 1013 Missense Mutation XP_016876706.1

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