Product Details

SNP ID

rs184923665

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8393377 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACACATGGCCACAGCTCAGCGTCC[A/G]GCTGGCGCCCTCCAGGTCCCGGAAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF222 PubMed Links

Gene Details

Gene

RNF222

Gene Name

ring finger protein 222

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146684.2	479	Missense Mutation	CGG,TGG	R29W	NP_001140156.1
XM_011523978.2	479	Missense Mutation	CGG,TGG	R29W	XP_011522280.1
XM_011523979.2	479	Missense Mutation	CGG,TGG	R29W	XP_011522281.1
XM_011523980.2	479	Missense Mutation	CGG,TGG	R29W	XP_011522282.1
XM_011523981.2	479	Missense Mutation	CGG,TGG	R29W	XP_011522283.1

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