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GGGCAGTGGGGCAGTCAGCTCCTGG[C/G]GCGGCAGCTGCAGGATTTCTGGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608123 MIM: 191039 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACOT8 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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ACOT8 - acyl-CoA thioesterase 8 | ||||||
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There are no transcripts associated with this gene. |
SNX21 - sorting nexin family member 21 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042632.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | NP_001036097.1 | |
NM_001042633.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | NP_001036098.1 | |
NM_033421.3 | 424 | Missense Mutation | GCG,GGG | A,G 112 | NP_219489.1 | |
NM_152897.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | NP_690857.1 | |
XM_005260608.4 | 424 | Intron | XP_005260665.1 | |||
XM_011529095.2 | 424 | Intron | XP_011527397.1 | |||
XM_011529096.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | XP_011527398.1 | |
XM_011529098.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | XP_011527400.1 | |
XM_011529099.2 | 424 | Missense Mutation | GCG,GGG | A,G 112 | XP_011527401.1 | |
XM_017028120.1 | 424 | Missense Mutation | GCG,GGG | A,G 112 | XP_016883609.1 |
TNNC2 - troponin C2, fast skeletal type | ||||||
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There are no transcripts associated with this gene. |