Product Details

SNP ID

rs1213184

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:12116647 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTAAAACATCGATCACGTGGCCTCA[A/G]AAATTCAGAGCCCGAGGGAGTGATA

Phenotype

MIM: 608881

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MICAL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs113945854] 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

MICAL2

Gene Name

microtubule associated monooxygenase, calponin and LIM domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282663.1		Intron			NP_001269592.1
NM_001282664.1		Intron			NP_001269593.1
NM_001282665.1		Intron			NP_001269594.1
NM_001282666.1		Intron			NP_001269595.1
NM_001282667.1		Intron			NP_001269596.1
NM_001282668.1		Intron			NP_001269597.1
NM_014632.3		Intron			NP_055447.1
XM_011520490.2		Intron			XP_011518792.1
XM_011520491.2		Intron			XP_011518793.1
XM_017018589.1		Intron			XP_016874078.1
XM_017018590.1		Intron			XP_016874079.1
XM_017018591.1		Intron			XP_016874080.1

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