Product Details

SNP ID

rs3776796

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:116084937 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCGGCGCCCGGGTCGCAGGAGACC[C/G]GGAGCCCTAAAACGGCCCCTGCGCG

Phenotype

MIM: 616704

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

COMMD10 PubMed Links

Additional Information

For this assay, SNP(s) [rs111808877] are located under a probe 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

COMMD10

Gene Name

COMM domain containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308080.1	346	Intron			NP_001295009.1
NM_016144.3	346	Intron			NP_057228.1
XM_011543458.2	346	UTR 5			XP_011541760.1
XM_011543460.2	346	UTR 5			XP_011541762.1
XM_017009553.1	346	Intron			XP_016865042.1
XM_017009555.1	346	UTR 5			XP_016865044.1
XM_017009556.1	346	UTR 5			XP_016865045.1
XM_017009557.1	346	Intron			XP_016865046.1

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