Product Details

SNP ID
rs143610472
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:19814645 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAGTAGGTGCGCGGCCAGGCGCC[A/G]GGCTGCCACGTGGTTTGCACTTACT
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_019062.1 634 Missense Mutation CGG,TGG R153W NP_061935.1

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