Product Details

SNP ID

rs4912755

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:139691066 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGTGATGGATCCGATGGCTCTGG[A/G]CCTGCTATCCAGCCAGCCCTCTTGA

Phenotype

MIM: 612752

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CXXC5 PubMed Links

Additional Information

For this assay, SNP(s) [rs116453062] 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

CXXC5

Gene Name

CXXC finger protein 5

There are no transcripts associated with this gene.

Gene

PSD2

Gene Name

pleckstrin and Sec7 domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032289.2		Intron			NP_115665.1
XM_011537696.2		Intron			XP_011535998.1
XM_017009975.1		Intron			XP_016865464.1
XM_017009976.1		Intron			XP_016865465.1
XM_017009977.1		Intron			XP_016865466.1

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