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CCTCAAAAATGATGCACCCCAAGCA[A/G]AACATAAAAAGAACAAAAAGAAAAA
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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There are no transcripts associated with this gene. |
CKMT2-AS1 - CKMT2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
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 | 659 | Missense Mutation | AAA,GAA | K,E 57 | NP_001124507.1 | |
NM_001131036.1 | 659 | Missense Mutation | AAA,GAA | K,E 57 | NP_001124508.1 | |
NM_032280.2 | 659 | Missense Mutation | AAA,GAA | K,E 57 | NP_115656.1 | |
XM_005248616.3 | 659 | Intron | XP_005248673.1 |