Product Details

SNP ID

rs34693363

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:19814766 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGACAGAGCGATACCTCTGTGCA[C/T]GGCTGGGCCAGCTGCCCCACCACCG

Phenotype

Polymorphism

C/T, 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	513	Silent Mutation	CCA,CCG	P112P	NP_061935.1

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