Product Details

SNP ID

rs2359661

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:31269826 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGTGAAGGACATAGCTGTCCCCAA[G/A]CAACCTCAATGGGAGAACACCCGGA

Phenotype

MIM: 120980

Polymorphism

G/A, Transition Substitution

Allele Nomenclature

Literature Links

ITGAM PubMed Links

Additional Information

For this assay, SNP(s) [rs72785590] 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

ITGAM

Gene Name

integrin subunit alpha M

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000632.3		Intron			NP_000623.2
NM_001145808.1		Intron			NP_001139280.1
XM_006721045.1		Intron			XP_006721108.1
XM_011545850.2		Intron			XP_011544152.1
XM_011545851.2		Intron			XP_011544153.1
XM_017023216.1		Intron			XP_016878705.1

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