Product Details

SNP ID

rs1971476

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113494637 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTGGGATGATAACAAAAAGTTCTA[A/G]AGATCTAGGTATTGTGGCATATATA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCUN1D2 PubMed Links

Additional Information

For this assay, SNP(s) [rs116043056] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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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