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ATAAGGACGGAGGTGATCCTCTATG[C/G]TGCCAACTGCCCAGTGGGTGAGCTG
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 |
---|---|---|
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 |
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 | 1501 | Missense Mutation | ACC,AGC | T,S 218 | NP_112201.1 | |
XM_005249433.3 | 1501 | Intron | XP_005249490.1 | |||
XM_011514928.2 | 1501 | Missense Mutation | ACC,AGC | T,S 189 | XP_011513230.1 |