Product Details

SNP ID
rs184794239
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:56923147 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGGTCACTCAGAGTGTAGGGCC[A/G]CGTGCTGATGCAGAGCATGGGCACT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MIER3 PubMed Links

Gene Details

Gene
MIER3
Gene Name
MIER family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297598.1 1697 Missense Mutation GCG,GTG A550V NP_001284527.1
NM_001297599.1 1697 Missense Mutation GCG,GTG A545V NP_001284528.1
NM_152622.4 1697 Missense Mutation GCG,GTG A544V NP_689835.3
XM_011543216.1 1697 Missense Mutation GCG,GTG A561V XP_011541518.1
XM_011543217.1 1697 Missense Mutation GCG,GTG A560V XP_011541519.1
XM_017009149.1 1697 Missense Mutation GCG,GTG A369V XP_016864638.1
Gene
SETD9
Gene Name
SET domain containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001171990.2 1697 Intron NP_001165461.1
NM_001323018.1 1697 Intron NP_001309947.1
NM_001323019.1 1697 Intron NP_001309948.1
NM_001323020.1 1697 Intron NP_001309949.1
NM_001323022.1 1697 Intron NP_001309951.1
NM_153706.3 1697 Intron NP_714917.2
XM_005248426.4 1697 Intron XP_005248483.1
XM_011543139.2 1697 Intron XP_011541441.1
XM_011543140.2 1697 Intron XP_011541442.1

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