Product Details

SNP ID

rs745182

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.10:80141966 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACTGACCCCCACCTGGGCCGTCCTC[C/T]GCTTGCTCCTGAGTTTGCTTTGAGG

Phenotype

MIM: 612857

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLAC9 PubMed Links

Additional Information

For this assay, SNP(s) [rs114929421] 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

PLAC9

Gene Name

placenta specific 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012973.1		Intron			NP_001012991.1

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