Product Details

SNP ID
rs201262383
Assay Type
Functionally tested
NCBI dbSNP Submissions
8
Location
Chr.1:19814802 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCCCCACCACCGCCTCATGGTC[A/G]CGCAGGCTGCAGATGAGGCCCCCGG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF186 PubMed Links

Gene Details

Gene
RNF186
Gene Name
ring finger protein 186
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019062.1 477 Silent Mutation CGC,CGT R100R NP_061935.1

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