Product Details

SNP ID

rs16827592

Assay Type

Functionally Tested

NCBI dbSNP Submissions

18

Location

Chr.1:161649251 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAGAGGATTGAAAGTAGAAGTGT[G/T]ATGAAACTCCTCTTTTACTTTTTTG

Phenotype

MIM: 604590

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

FCGR2B PubMed Links

Additional Information

For this assay, SNP(s) [rs61089283] 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

FCGR2B

Gene Name

Fc fragment of IgG receptor IIb

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002273.2		Intron			NP_001002273.1
NM_001002274.2		Intron			NP_001002274.1
NM_001002275.2		Intron			NP_001002275.1
NM_001190828.1		Intron			NP_001177757.1
NM_004001.4		Intron			NP_003992.3
XM_011509292.2		Intron			XP_011507594.1
XM_017000669.1		Intron			XP_016856158.1
XM_017000670.1		Intron			XP_016856159.1
XM_017000671.1		Intron			XP_016856160.1
XM_017000672.1		Intron			XP_016856161.1

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