Product Details

SNP ID

rs684

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:44886246 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCGGCCATGGCTGTCATTTTGAGGG[C/T]GGAAAATAACTGGATTTCTGGTTAA

Phenotype

MIM: 600065

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ITGB2 PubMed Links

Additional Information

For this assay, SNP(s) [rs375146934] 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

ITGB2

Gene Name

integrin subunit beta 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000211.4	2682	UTR 3			NP_000202.3
NM_001127491.2	2682	UTR 3			NP_001120963.2
NM_001303238.1	2682	UTR 3			NP_001290167.1
XM_006724001.1	2682	UTR 3			XP_006724064.1
XM_017028341.1	2682	UTR 3			XP_016883830.1

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