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GTTCCTGTGGCAGGTAGAGGCAGAT[A/G]CTGCATAACTTGAAGATTGTAGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615652 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACOT13 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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ACOT13 - acyl-CoA thioesterase 13 | ||||||
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There are no transcripts associated with this gene. |
C6orf62 - chromosome 6 open reading frame 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030939.4 | 1451 | Silent Mutation | AGC,AGT | S,S 201 | NP_112201.1 | |
XM_005249433.3 | 1451 | Intron | XP_005249490.1 | |||
XM_011514928.2 | 1451 | Silent Mutation | AGC,AGT | S,S 172 | XP_011513230.1 |