Product Details

SNP ID
rs2882853
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:90193137 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTACTCCCTTTCCAAGCTGCCTCC[C/T]GAGCTCTTTATAAACACTGGCATTC
Phenotype
MIM: 617029
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SEMA4B PubMed Links
Additional Information
For this assay, SNP(s) [rs192394015,rs531339835] 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
SEMA4B
Gene Name
semaphorin 4B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324029.1 Intron NP_001310958.1
NM_001324030.1 Intron NP_001310959.1
NM_001324031.1 Intron NP_001310960.1
NM_001324032.1 Intron NP_001310961.1
NM_001324033.1 Intron NP_001310962.1
NM_001324034.1 Intron NP_001310963.1
NM_020210.3 Intron NP_064595.2
NM_198925.2 Intron NP_945119.1

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