Product Details

SNP ID

rs10187661

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:106073832 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATGTATAACAGGGATTCACCGCAA[C/G]TGAGGAAGGAAGTCATTCTTTGTGC

Phenotype

MIM: 611752

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

C2orf40 PubMed Links

Additional Information

For this assay, SNP(s) [rs72034828] are located under a probe and SNP(s) [rs137908864] 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

C2orf40

Gene Name

chromosome 2 open reading frame 40

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032411.2		Intron			NP_115787.1
XM_006712799.3		Intron			XP_006712862.1
XM_011511993.2		Intron			XP_011510295.1
XM_017005106.1		Intron			XP_016860595.1

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