Product Details

SNP ID

rs10222765

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:76229931 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCCTTGGAGCAGGGTTATTCTGT[C/T]ATTAATTGCTATTATGTCCTGAGGT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM47E PubMed Links

Additional Information

For this assay, SNP(s) [rs115105683,rs77514904] 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

FAM47E

Gene Name

family with sequence similarity 47 member E

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136570.2		Intron			NP_001130042.1
NM_001242936.1		Intron			NP_001229865.1

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