Product Details

SNP ID

rs138609958

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:20862383 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCGGCCTTCTTGGTCCCGTTGAC[A/G]AGGATATCTCCACCTGGCTTGCCAC

Phenotype

MIM: 616167

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DCUN1D3 PubMed Links

Gene Details

Gene

DCUN1D3

Gene Name

defective in cullin neddylation 1 domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173475.3	416	Silent Mutation	CTC,CTT	L52L	NP_775746.1

View Full Product Details