Product Details

SNP ID
rs77435097
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:8393064 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCAGCAGGTCCAGGGGGAGCTGG[A/G]CGCTCTGGCCCGGGCTGCCTGGCGG
Phenotype
MIM: 603704
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RNF222 PubMed Links
Additional Information
For this assay, SNP(s) [rs12601362] 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
RNF222
Gene Name
ring finger protein 222
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146684.2 792 Missense Mutation GCC,GTC A133V NP_001140156.1
XM_011523978.2 792 Missense Mutation GCC,GTC A133V XP_011522280.1
XM_011523979.2 792 Missense Mutation GCC,GTC A133V XP_011522281.1
XM_011523980.2 792 Missense Mutation GCC,GTC A133V XP_011522282.1
XM_011523981.2 792 Missense Mutation GCC,GTC A133V XP_011522283.1
Gene
RPL26
Gene Name
ribosomal protein L26
There are no transcripts associated with this gene.

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