Product Details

SNP ID

rs8037630

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:80782731 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAGCTCAGAAGGAATCTTAGCTTC[C/T]TCCGTCTAAAAGGATTGGAGCTGAA

Phenotype

MIM: 608366

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CEMIP PubMed Links

Additional Information

For this assay, SNP(s) [rs139273333] 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

CEMIP

Gene Name

cell migration inducing hyaluronan binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001293298.1		Intron			NP_001280227.1
NM_001293304.1		Intron			NP_001280233.1
NM_018689.2		Intron			NP_061159.1

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