Product Details

SNP ID
rs116149438
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:113494804 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATTTCGTTTCTGGAGTGACGTTGA[A/G]CATGGTGTCCCCAAGCAACCCAGTG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DCUN1D2 PubMed Links

Gene Details

Gene
DCUN1D2
Gene Name
defective in cullin neddylation 1 domain containing 2
There are no transcripts associated with this gene.

Gene
TMCO3
Gene Name
transmembrane and coiled-coil domains 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017905.4 Intron NP_060375.4
XM_006719969.1 Intron XP_006720032.1
XM_011537498.2 Intron XP_011535800.1
XM_011537501.2 Intron XP_011535803.1
XM_011537502.2 Intron XP_011535804.1
XM_011537504.2 Intron XP_011535806.1
XM_011537506.2 Intron XP_011535808.1
XM_011537507.2 Intron XP_011535809.1
XM_011537509.2 Intron XP_011535811.1
XM_017020629.1 Intron XP_016876118.1
XM_017020630.1 Intron XP_016876119.1
XM_017020631.1 Intron XP_016876120.1
XM_017020632.1 Intron XP_016876121.1
XM_017020633.1 Intron XP_016876122.1
XM_017020634.1 Intron XP_016876123.1
XM_017020635.1 Intron XP_016876124.1
XM_017020636.1 Intron XP_016876125.1

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