Search Thermo Fisher Scientific
- SNP ID:
- rs1799853
- Gene
-
CYP2C9 - Gene Name
- cytochrome P450 family 2 subfamily C member 9
- Set Membership:
- > HapMap > DME > Validated > Inventoried
- Chromosome Location:
- Chr.10: 94942290 - 94942290 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GATGGGGAAGAGGAGCATTGAGGAC[C/T]GTGTTCAAGAGGAAGCCCGCTGCCT
Genomic Map
Back To TopAssay Details
Species: |
Human |
dbSNP Submissions: |
NA
|
Phenotype: |
MIM: 601130
|
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
|
Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU)
|
|||||||||
EAS
|
African American
|
YRI (Yoruba) - Not Available | |||||||||
SAS
|
Japanese
|
CHB (Han Chinese) - Not Available | |||||||||
AFR
|
Chinese
|
JPT (Japanese) - Not Available | |||||||||
EUR
|
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AMR
|
| 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 | |
Back To TopMore Information
Set Membership: |
HapMap
DME
Validated
Inventoried
|
Panther Classification:
Gene Ontology Categories:
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