Product Details

SNP ID
rs12601362
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:8393065 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGCAGGTCCAGGGGGAGCTGGG[C/T]GCTCTGGCCCGGGCTGCCTGGCGGC
Phenotype
MIM: 603704
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF222 PubMed Links

Gene Details

Gene
RNF222
Gene Name
ring finger protein 222
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146684.2 791 Missense Mutation ACC,GCC T133A NP_001140156.1
XM_011523978.2 791 Missense Mutation ACC,GCC T133A XP_011522280.1
XM_011523979.2 791 Missense Mutation ACC,GCC T133A XP_011522281.1
XM_011523980.2 791 Missense Mutation ACC,GCC T133A XP_011522282.1
XM_011523981.2 791 Missense Mutation ACC,GCC T133A XP_011522283.1
Gene
RPL26
Gene Name
ribosomal protein L26
There are no transcripts associated with this gene.

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