Product Details

SNP ID
rs11715452
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:122909863 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAATGCCCAGTAGGTCCACAGCCCA[G/T]GCATGGCAGCATAGTGTCAGCGTGA
Phenotype
MIM: 609298
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SEMA5B PubMed Links
Additional Information
For this assay, SNP(s) [rs75990321] 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
SEMA5B
Gene Name
semaphorin 5B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031702.3 4173 UTR 3 NP_001026872.2
NM_001256346.1 4173 UTR 3 NP_001243275.1
NM_001256347.1 4173 UTR 3 NP_001243276.1
NM_001256348.1 4173 UTR 3 NP_001243277.1
XM_017006638.1 4173 UTR 3 XP_016862127.1
XM_017006639.1 4173 Intron XP_016862128.1

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