Product Details

SNP ID

rs138295711

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113495639 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGTTTCCCGTCCTTCCCTGGGCG[A/G]TGCAGGCTGTGGAGCACGAGGAGGT

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	419	Missense Mutation	ATG,GTG	M20V	NP_060375.4
XM_006719969.1	419	Missense Mutation	ATG,GTG	M20V	XP_006720032.1
XM_011537498.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535800.1
XM_011537501.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535803.1
XM_011537502.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535804.1
XM_011537504.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535806.1
XM_011537506.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535808.1
XM_011537507.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535809.1
XM_011537509.2	419	Missense Mutation	ATG,GTG	M20V	XP_011535811.1
XM_017020629.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876118.1
XM_017020630.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876119.1
XM_017020631.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876120.1
XM_017020632.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876121.1
XM_017020633.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876122.1
XM_017020634.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876123.1
XM_017020635.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876124.1
XM_017020636.1	419	Missense Mutation	ATG,GTG	M20V	XP_016876125.1

View Full Product Details