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TCTACCTTAGGACTGATTCTAGTTT[C/T]GTGGGGCTTTTGGGGGTGGGGGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608881 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MICAL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MICAL2 - microtubule associated monooxygenase, calponin and LIM domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |