Product Details

SNP ID
rs104894493
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:71811591 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGGCTTCTTCAAGAGGAGCGTAC[A/G]GCGGAGGCTCATCTACAGGTGAGTG
Phenotype
MIM: 604485
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NR2E3 PubMed Links

Gene Details

Gene
NR2E3
Gene Name
nuclear receptor subfamily 2 group E member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014249.3 423 Missense Mutation CAG,CGG Q76R NP_055064.1
NM_016346.3 423 Missense Mutation CAG,CGG Q76R NP_057430.1

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