Product Details

SNP ID
rs148594830
Assay Type
Functionally tested
NCBI dbSNP Submissions
7
Location
Chr.1:19814752 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCCACCAGCCCCTGAGGACAGAGC[A/G]ATACCTCTGTGCATGGCTGGGCCAG
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_019062.1 527 Missense Mutation TCG,TTG S117L NP_061935.1

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