Product Details

SNP ID
rs7812958
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:33549823 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACAGAAGTTTCCACTGCACTGGAAA[G/T]TACTGTCCTAGAAGAATGGTTTTCA
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
RNF122 PubMed Links
Additional Information
For this assay, SNP(s) [rs76470057] are located under a probe and SNP(s) [rs138344299] are located under a primer 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
RNF122
Gene Name
ring finger protein 122
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024787.3 Intron NP_079063.2
XM_017013846.1 Intron XP_016869335.1

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