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GCAGCCTCCAGGTCCTTGTCCTCCT[C/G]TCTCTCCCGGAGCCGCTGCTCCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608882 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MICAL3 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
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
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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MICAL3 - microtubule associated monooxygenase, calponin and LIM domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122731.2 | 6666 | Intron | NP_001116203.1 | |||
NM_001136004.3 | 6666 | Intron | NP_001129476.1 | |||
NM_015241.2 | 6666 | Missense Mutation | CAG,GAG | Q,E 1983 | NP_056056.2 | |
XM_005261262.3 | 6666 | Missense Mutation | CAG,GAG | Q,E 1983 | XP_005261319.1 | |
XM_011546137.2 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_011544439.1 | |
XM_011546139.2 | 6666 | Missense Mutation | CAG,GAG | Q,E 2173 | XP_011544441.1 | |
XM_011546142.2 | 6666 | Missense Mutation | CAG,GAG | Q,E 2156 | XP_011544444.1 | |
XM_011546146.2 | 6666 | Intron | XP_011544448.1 | |||
XM_017028865.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884354.1 | |
XM_017028866.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884355.1 | |
XM_017028867.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884356.1 | |
XM_017028868.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884357.1 | |
XM_017028869.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884358.1 | |
XM_017028870.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2190 | XP_016884359.1 | |
XM_017028871.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2189 | XP_016884360.1 | |
XM_017028872.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2173 | XP_016884361.1 | |
XM_017028873.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2169 | XP_016884362.1 | |
XM_017028874.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2162 | XP_016884363.1 | |
XM_017028875.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2154 | XP_016884364.1 | |
XM_017028876.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2144 | XP_016884365.1 | |
XM_017028877.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2123 | XP_016884366.1 | |
XM_017028878.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2085 | XP_016884367.1 | |
XM_017028879.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2038 | XP_016884368.1 | |
XM_017028880.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2038 | XP_016884369.1 | |
XM_017028881.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2038 | XP_016884370.1 | |
XM_017028882.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 2017 | XP_016884371.1 | |
XM_017028883.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 1890 | XP_016884372.1 | |
XM_017028884.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 1738 | XP_016884373.1 | |
XM_017028885.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 1289 | XP_016884374.1 | |
XM_017028886.1 | 6666 | Missense Mutation | CAG,GAG | Q,E 1289 | XP_016884375.1 | |
XM_017028887.1 | 6666 | Intron | XP_016884376.1 |