Product Details

SNP ID
rs797017
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:118964526 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTAAAATGAACATATAAATAATTC[A/G]TAAGTTTTAGTGCTAGATTATTAAA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FAM184A PubMed Links
Additional Information
For this assay, SNP(s) [rs201989692] 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
FAM184A
Gene Name
family with sequence similarity 184 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001100411.2 Intron NP_001093881.1
NM_001288576.1 Intron NP_001275505.1
NM_024581.5 Intron NP_078857.5

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