Product Details

SNP ID
hCV25989459
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:185367349 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATTCATTTTTAAGAATAGTAAAGT[A/C]CAGTGAATTTCAAGAAAATTTGTTA
Phenotype
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
LRP2BP PubMed Links
Additional Information
For this assay, SNP(s) [rs77624707] 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
LRP2BP
Gene Name
LRP2 binding protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018409.3 Intron NP_060879.2
Gene
SNX25
Gene Name
sorting nexin 25
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317781.1 Intron NP_001304710.1

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