Product Details

SNP ID: rs199765506
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:20860336 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACAGATTCCGTCAATGCTGTCTGC[A/C]CTTATTGCTTTGCAGCCATCAAAAA
Phenotype: MIM: 616167
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: DCUN1D3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173475.3	725	Missense Mutation	AGG,AGT	R155S	NP_775746.1