Product Details

SNP ID

rs17164382

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:1167402 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCCTGTGCCCTCGGCCGCCTGCAG[C/T]ATGAGCCTGCACAGGAGCCCCCGAC

Phenotype

MIM: 605918

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SPON2 PubMed Links

Additional Information

For this assay, SNP(s) [rs77549869] 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

SPON2

Gene Name

spondin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128325.2	1395	UTR 3			NP_001121797.1
NM_001199021.1	1395	UTR 3			NP_001185950.1
NM_012445.3	1395	UTR 3			NP_036577.1

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