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GAGCAGGTCCAGGTAGGCTGTTCTT[G/T]CCATGTCCACTTGGGCACCAGACAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601641 | |||||||||||||||||||||||
Literature Links: |
ACOX2 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 - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
ACOX2 - acyl-CoA oxidase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003500.3 | 1991 | Missense Mutation | GAA,GCA | E,A 605 | NP_003491.1 | |
XM_005265505.1 | 1991 | Missense Mutation | GAA,GCA | E,A 605 | XP_005265562.1 | |
XM_006713340.3 | 1991 | Missense Mutation | GAA,GCA | E,A 507 | XP_006713403.1 | |
XM_017007302.1 | 1991 | Missense Mutation | GAA,GCA | E,A 535 | XP_016862791.1 |