Product Details

SNP ID

rs3815019

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:20904964 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTATATTTCCAGTAAGAAGTATGC[A/G]CTGTGGTCTGAAGATAAGCGGTGCT

Phenotype

MIM: 616167 MIM: 614709

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCUN1D3 PubMed Links

Additional Information

For this assay, SNP(s) [rs115829564] 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

DCUN1D3

Gene Name

defective in cullin neddylation 1 domain containing 3

There are no transcripts associated with this gene.

Gene

LYRM1

Gene Name

LYR motif containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128301.2		Intron			NP_001121773.1
NM_001128302.2		Intron			NP_001121774.1
NM_001302835.1		Intron			NP_001289764.1
NM_001302836.1		Intron			NP_001289765.1
NM_020424.4		Intron			NP_065157.1
XM_005255444.1		Intron			XP_005255501.1
XM_011545900.2		Intron			XP_011544202.1
XM_011545901.2		Intron			XP_011544203.1
XM_011545902.1		Intron			XP_011544204.1
XM_011545908.2		Intron			XP_011544210.1
XM_017023475.1		Intron			XP_016878964.1
XM_017023476.1		Intron			XP_016878965.1
XM_017023477.1		Intron			XP_016878966.1
XM_017023478.1		Intron			XP_016878967.1
XM_017023479.1		Intron			XP_016878968.1
XM_017023480.1		Intron			XP_016878969.1
XM_017023481.1		Intron			XP_016878970.1
XM_017023482.1		Intron			XP_016878971.1

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