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GAAGTAGTCACTTTTCTTAAAGTTG[A/C]CATTCTTATCTAGAAAGTGGCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601129 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP2C8 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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CYP2C8 - cytochrome P450 family 2 subfamily C member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000770.3 | 1345 | Missense Mutation | GGC,GTC | G,V 417 | NP_000761.3 | |
NM_001198853.1 | 1345 | Missense Mutation | GGC,GTC | G,V 347 | NP_001185782.1 | |
NM_001198854.1 | 1345 | Missense Mutation | GGC,GTC | G,V 315 | NP_001185783.1 | |
NM_001198855.1 | 1345 | Missense Mutation | GGC,GTC | G,V 347 | NP_001185784.1 |