Product Details

SNP ID

rs199540262

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:19814495 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGAGGAGGGCCAGCAGCTGCCCC[G/T]GGTGCTGGGGAGACAGCAGAAGAGG

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	784	Silent Mutation	GGG,TGG	G203W	NP_061935.1

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