Product Details

SNP ID
hCV28032675
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:33554615 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGCAAAAACCCTGGGCAATCCCAG[C/G]TGGGGACCTAGTACCAACCAGTCTG
Phenotype
Polymorphism
C/G, 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 Intron NP_079063.2

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