Product Details

SNP ID

rs141431566

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:33551072 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATATAATTGTAACTTCTTGGCATCA[C/T]CTTTAAGCACCACCTGAAAAGAAAG

Phenotype

Polymorphism

C/T, 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	647	Missense Mutation			NP_079063.2
XM_017013846.1	647	Missense Mutation			XP_016869335.1

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