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- SNP ID:
- rs117111102
- Gene
-
CYP2C18 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 94688163 - 94688163 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CAATGGAAAGAGATGGAAGGAGATC[C/T]GGCGTTTCTGCCTCATGACTCTGCG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601131
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Literature Links: |
CYP2C18 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
| CYP2C18 - cytochrome P450 family 2 subfamily C member 18 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000772.2 | 696 | Missense Mutation | CGG,TGG | R,W 124 | NP_000763.1 | |
| NM_001128925.1 | 696 | Missense Mutation | CGG,TGG | R,W 124 | NP_001122397.1 | |
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