Product Details

SNP ID

rs1566576

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51217369 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCTGAACATCTCACTCTTTCGAA[A/T]CTCCAATGTCTTTTTTGTTTTTGTT

Phenotype

MIM: 159590

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CD33 PubMed Links

Additional Information

For this assay, SNP(s) [rs116623489] 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

CD33

Gene Name

CD33 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001082618.1		Intron			NP_001076087.1
NM_001177608.1		Intron			NP_001171079.1
NM_001772.3		Intron			NP_001763.3
XM_011527531.2		Intron			XP_011525833.1
XM_011527532.2		Intron			XP_011525834.1
XM_017027508.1		Intron			XP_016882997.1
XM_017027509.1		Intron			XP_016882998.1
XM_017027510.1		Intron			XP_016882999.1

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