Product Details

SNP ID

rs147098542

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:33548841 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGTTACACATGGGGCAGACACAG[A/C]GAACTTCCAGCCATTTCACCAGACA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

RNF122 PubMed Links

Gene Details

Gene

RNF122

Gene Name

ring finger protein 122

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024787.3	785	Missense Mutation	CGC,CTC	R127L	NP_079063.2
XM_017013846.1	785	Missense Mutation	CGC,CTC	R103L	XP_016869335.1

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