Product Details

SNP ID
rs17675862
Assay Type
Functionally Tested
NCBI dbSNP Submissions
31
Location
Chr.1:157678489 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCTGCCTTGCCACGTGTCTCCACT[A/G]TGAAAATAACACAGTGCTTGCTCAG
Phenotype
MIM: 606510
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FCRL3 PubMed Links
Additional Information
For this assay, SNP(s) [rs16838952] 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
FCRL3
Gene Name
Fc receptor like 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320333.1 2648 Intron NP_001307262.1
NM_052939.3 2648 UTR 3 NP_443171.2
XM_006711145.1 2648 UTR 3 XP_006711208.1

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