Product Details

SNP ID
rs7591605
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:131113716 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGAGCTAGAGTCTGAGAAGTAAGG[A/C]AGAAGATGGAGAATTTGACTTTCAC
Phenotype
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
PLEKHB2 PubMed Links
Additional Information
For this assay, SNP(s) [rs111559310] 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
PLEKHB2
Gene Name
pleckstrin homology domain containing B2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001100623.1 Intron NP_001094093.1
NM_001267062.1 Intron NP_001253991.1
NM_001267063.1 Intron NP_001253992.1
NM_001267064.1 Intron NP_001253993.1
NM_001267065.1 Intron NP_001253994.1
NM_001267066.1 Intron NP_001253995.1
NM_001267067.1 Intron NP_001253996.1
NM_001267068.1 Intron NP_001253997.1
NM_001309448.1 Intron NP_001296377.1
NM_001309450.1 Intron NP_001296379.1
NM_001309451.1 Intron NP_001296380.1
NM_001309452.1 Intron NP_001296381.1
NM_017958.2 Intron NP_060428.2
XM_011511385.2 Intron XP_011509687.1
XM_011511386.2 Intron XP_011509688.1
XM_017004408.1 Intron XP_016859897.1
XM_017004409.1 Intron XP_016859898.1
XM_017004410.1 Intron XP_016859899.1
XM_017004411.1 Intron XP_016859900.1
XM_017004412.1 Intron XP_016859901.1
XM_017004413.1 Intron XP_016859902.1
Gene
POTEI
Gene Name
POTE ankyrin domain family member I
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001277406.1 Intron NP_001264335.1
XM_011511670.2 Intron XP_011509972.1
XM_017004732.1 Intron XP_016860221.1
XM_017004733.1 Intron XP_016860222.1
XM_017004734.1 Intron XP_016860223.1
XM_017004735.1 Intron XP_016860224.1

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