Product Details

SNP ID

rs138789031

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:20862269 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTAGCGCCTGAACAGTTCTTCCAA[A/T]CTTTGCAAGGAAGACTCCTCGGCAT

Phenotype

MIM: 616167

Polymorphism

A/T, Transversion 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	530	Missense Mutation	AGA,AGT	R90S	NP_775746.1

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