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GGGATGGCCGGAGGGCTGCGGGCTC[C/T]GCTATTTGCAAATGGATGCCCCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 606803 | ||||||||||||||||||||
Literature Links: |
ACOT11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
ACOT11 - acyl-CoA thioesterase 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015547.3 | 1456 | Intron | NP_056362.1 | |||
NM_147161.3 | 1456 | UTR 3 | NP_671517.1 |
FAM151A - family with sequence similarity 151 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_176782.2 | 1456 | Intron | NP_788954.2 | |||
XM_006710599.3 | 1456 | Silent Mutation | GCA,GCG | A,A 390 | XP_006710662.1 |