Product Details

SNP ID

rs77435097

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8393064 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCAGCAGGTCCAGGGGGAGCTGG[A/G]CGCTCTGGCCCGGGCTGCCTGGCGG

Phenotype

MIM: 603704

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RNF222 PubMed Links

Additional Information

For this assay, SNP(s) [rs12601362] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	792	Missense Mutation	GCC,GTC	A133V	NP_001140156.1
XM_011523978.2	792	Missense Mutation	GCC,GTC	A133V	XP_011522280.1
XM_011523979.2	792	Missense Mutation	GCC,GTC	A133V	XP_011522281.1
XM_011523980.2	792	Missense Mutation	GCC,GTC	A133V	XP_011522282.1
XM_011523981.2	792	Missense Mutation	GCC,GTC	A133V	XP_011522283.1

Gene

RPL26

Gene Name

ribosomal protein L26

There are no transcripts associated with this gene.

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