Product Details

SNP ID

rs4821566

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36918465 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGATCATCCTCATATTCTTGCAAGA[C/G]GAAAAGTTTACCAGTGAGAACTAGG

Phenotype

MIM: 138981

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CSF2RB PubMed Links

Additional Information

For this assay, SNP(s) [rs146725820] 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

CSF2RB

Gene Name

colony stimulating factor 2 receptor beta common subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000395.2		Intron			NP_000386.1
XM_005261340.3		Intron			XP_005261397.1
XM_011529903.2		Intron			XP_011528205.1
XM_011529904.2		Intron			XP_011528206.1
XM_011529905.2		Intron			XP_011528207.1

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