Product Details

SNP ID

rs16840057

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:207823806 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTAGGAGGGTATCCCATACTCTTG[C/T]CTTTTACCTAGAGTTTAACAATGAC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLEKHM3 PubMed Links

Additional Information

For this assay, SNP(s) [rs78651674] 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

PLEKHM3

Gene Name

pleckstrin homology domain containing M3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080475.2	7289	UTR 3			NP_001073944.1
XM_005246545.3	7289	UTR 3			XP_005246602.1
XM_006712521.3	7289	Intron			XP_006712584.1
XM_011511160.2	7289	UTR 3			XP_011509462.1
XM_011511163.2	7289	Intron			XP_011509465.1
XM_017004071.1	7289	Intron			XP_016859560.1
XM_017004072.1	7289	UTR 3			XP_016859561.1
XM_017004073.1	7289	UTR 3			XP_016859562.1

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