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GCGCTTCTTGGATTTTCCAAAGGAG[G/T]TGACCTGTGTCTCTCAATGGCTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614267 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACOT6 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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ACOT6 - acyl-CoA thioesterase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037162.1 | 393 | Missense Mutation | GGT,GTT | G,V 21 | NP_001032239.1 | |
XM_011537076.2 | 393 | Missense Mutation | GGT,GTT | G,V 273 | XP_011535378.1 |
HEATR4 - HEAT repeat containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220484.1 | 393 | Intron | NP_001207413.1 | |||
NM_203309.2 | 393 | Intron | NP_976054.2 | |||
XM_006720143.2 | 393 | Intron | XP_006720206.1 | |||
XM_011536760.2 | 393 | Intron | XP_011535062.1 | |||
XM_011536761.2 | 393 | Intron | XP_011535063.1 | |||
XM_017021289.1 | 393 | Intron | XP_016876778.1 |