Product Details

SNP ID
rs138459633
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:182834856 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTTGTATTTCGGGATTTAGTTG[C/T]GTGCTTGCCGGGGGTTCGAGTTCCT
Phenotype
MIM: 605083
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FRZB PubMed Links
Additional Information
For this assay, SNP(s) [rs7775] are located under a probe 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
FRZB
Gene Name
frizzled-related protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001463.3 1189 Missense Mutation CAC,CGC H324R NP_001454.2

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