Product Details

SNP ID

rs78512177

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8392857 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGATGGCGGCCACCACGGCCACC[A/G]CAGCGATGAGCGTGATGAGCAGCAG

Phenotype

MIM: 603704

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	999	Missense Mutation	GCG,GTG	A202V	NP_001140156.1
XM_011523978.2	999	Missense Mutation	GCG,GTG	A202V	XP_011522280.1
XM_011523979.2	999	Missense Mutation	GCG,GTG	A202V	XP_011522281.1
XM_011523980.2	999	Missense Mutation	GCG,GTG	A202V	XP_011522282.1
XM_011523981.2	999	Missense Mutation	GCG,GTG	A202V	XP_011522283.1

Gene

RPL26

Gene Name

ribosomal protein L26

There are no transcripts associated with this gene.

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