Product Details

SNP ID

rs11859533

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:89577124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGCAGTTGGACCAGGGAACTGCA[C/T]GGGATGGGAGAGGCTGGTGAGCCCA

Phenotype

MIM: 605689

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CPNE7 PubMed Links

Additional Information

For this assay, SNP(s) [rs559574160] 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

CPNE7

Gene Name

copine 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014427.4		Intron			NP_055242.1
NM_153636.2		Intron			NP_705900.1
XM_011523000.1		Intron			XP_011521302.1
XM_011523001.2		Intron			XP_011521303.1
XM_017023138.1		Intron			XP_016878627.1
XM_017023139.1		Intron			XP_016878628.1
XM_017023140.1		Intron			XP_016878629.1
XM_017023141.1		Intron			XP_016878630.1

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