Product Details

SNP ID

rs2914944

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:93711815 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TATTCTGATCTTTGGGCTCACTTCT[A/G]TGTTCTGCCTGGATGCTGGTTTTAA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM92A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs115643793] 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

FAM92A1

Gene Name

family with sequence similarity 92 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283034.1		Intron			NP_001269963.1
NM_145269.4		Intron			NP_660312.2
XM_005250787.2		Intron			XP_005250844.1

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