Product Details

SNP ID

rs201080415

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:86048607 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGAGGCCCTCTGCATGAGGTTT[C/T]GGGATATGGCCCTCTGGAGATTCTT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PSKH2 PubMed Links

Additional Information

For this assay, SNP(s) [rs16876805] 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

PSKH2

Gene Name

protein serine kinase H2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033126.1	1013	Missense Mutation	CAA,CGA	Q338R	NP_149117.1
XM_017013929.1	1013	Missense Mutation	CAA,CGA	Q457R	XP_016869418.1

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