Product Details

SNP ID
rs2307072
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:12110991 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCGGCACGCCGAACTACCTCTTAC[C/T]CCGCTCCGCAACACCCAAACCCTGC
Phenotype
MIM: 608881
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MICAL2 PubMed Links

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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