Product Details

SNP ID

rs144271550

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:33549434 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGCGGTGAAAGGCGTGTTGGCAC[A/G]GGAGCACGCCTAACTCATCCTTCCC

Phenotype

Polymorphism

A/G, Transition 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	734	Missense Mutation	CCG,CTG	P110L	NP_079063.2
XM_017013846.1	734	Missense Mutation	CCG,CTG	P86L	XP_016869335.1

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