Product Details

SNP ID

rs7566028

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:11139537 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTACCTCTCCCTAGCCTTCCTCT[A/G]TCACTCACATTGGAAAGTTACAAAG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C2orf50 PubMed Links

Additional Information

For this assay, SNP(s) [rs76491752] 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

C2orf50

Gene Name

chromosome 2 open reading frame 50

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182500.2		Intron			NP_872306.1
XM_006711857.2		Intron			XP_006711920.1
XM_006711858.2		Intron			XP_006711921.1
XM_006711859.3		Intron			XP_006711922.1

Gene

FLJ33534

Gene Name

uncharacterized LOC285150

There are no transcripts associated with this gene.

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