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CYP2C9
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601130
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Literature Links: |
CYP2C9 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
CYP2C9*2A,c.430C>T
CYP2C9*2A,g.3608C>T
CYP2C9*2B,c.430C>T
CYP2C9*2B,g.3608C>T
CYP2C9*2C,c.430C>T
CYP2C9*2C,g.3608C>T
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
Global
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Caucasian
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba) - Not Available | |||||||||
SAS
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Japanese
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CHB (Han Chinese) - Not Available | |||||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | |||||||||
EUR
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AMR
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| CYP2C9 - cytochrome P450 family 2 subfamily C member 9 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000771.3 | 455 | Missense Mutation | CGT,TGT | R,C 144 | NP_000762.2 | |
| XM_017015758.1 | 455 | Missense Mutation | CGT,TGT | R,C 144 | XP_016871247.1 | |
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Set Membership: |
HapMap
DME
Validated
Inventoried
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Panther Classification:
Gene Ontology Categories:
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