Product Details

SNP ID
rs35541730
Assay Type
Functionally tested
NCBI dbSNP Submissions
34
Location
Chr.1:19814480 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCAGAAGAGAGTCCTGGAGGAGG[G/T]CCAGCAGCTGCCCCGGGTGCTGGGG
Phenotype
Polymorphism
G/T, Transversion 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_019062.1 799 Missense Mutation ACC,CCC T208P NP_061935.1

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