Product Details

SNP ID

rs11807921

Assay Type

Functionally Tested

NCBI dbSNP Submissions

14

Location

Chr.1:220754675 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACTAAGCAGTGAGGGAGAGTCTCT[C/G]AGCCAGGCTCATGTTCTTGTTTTTG

Phenotype

MIM: 614127

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MARC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs201384609] 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

MARC2

Gene Name

mitochondrial amidoxime reducing component 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317338.1		Intron			NP_001304267.1
NM_017898.4		Intron			NP_060368.2
XM_006711407.2		Intron			XP_006711470.1
XM_011509684.1		Intron			XP_011507986.1
XM_017001581.1		Intron			XP_016857070.1

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