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TTTTCTATTCCTTTACAGAGCGAAT[C/G]GTCACAGTTGGTCGCTGGGCAAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614315 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACOT12 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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ACOT12 - acyl-CoA thioesterase 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_130767.2 | 1195 | Intron | NP_570123.1 | |||
XM_006714531.2 | 1195 | Intron | XP_006714594.1 | |||
XM_006714532.3 | 1195 | Intron | XP_006714595.1 | |||
XM_017009045.1 | 1195 | Intron | XP_016864534.1 | |||
XM_017009046.1 | 1195 | Intron | XP_016864535.1 | |||
XM_017009047.1 | 1195 | Intron | XP_016864536.1 | |||
XM_017009048.1 | 1195 | Intron | XP_016864537.1 |
ZCCHC9 - zinc finger CCHC-type containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001131035.1 | 1195 | Missense Mutation | ATC,ATG | I,M 235 | NP_001124507.1 | |
NM_001131036.1 | 1195 | Missense Mutation | ATC,ATG | I,M 235 | NP_001124508.1 | |
NM_032280.2 | 1195 | Missense Mutation | ATC,ATG | I,M 235 | NP_115656.1 | |
XM_005248616.3 | 1195 | Missense Mutation | ATC,ATG | I,M 84 | XP_005248673.1 |