Product Details

SNP ID
rs572378
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:103054985 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCTTATCCAAAATGCTTGGGACCG[A/G]AAGTGTTTTAGATTTCTTTTTTTTG
Phenotype
MIM: 616522
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DCUN1D5 PubMed Links

Gene Details

Gene
DCUN1D5
Gene Name
defective in cullin neddylation 1 domain containing 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318739.1 8534 UTR 3 NP_001305668.1
NM_001318740.1 8534 UTR 3 NP_001305669.1
NM_001318741.1 8534 UTR 3 NP_001305670.1
NM_032299.3 8534 UTR 3 NP_115675.1
XM_017018404.1 8534 Intron XP_016873893.1

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