Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGCCTCCGGGACCCAGACCCCTC[C/T]CAATCCTGGGAAACCTGCTGCTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 124070 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP2F1 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
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CEPH (CEU) - Not Available | ||||||
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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CYP2F1 - cytochrome P450 family 2 subfamily F member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000774.4 | 324 | Missense Mutation | CCA,TCA | P,S 38 | NP_000765.2 | |
XM_011526551.2 | 324 | Missense Mutation | CCA,TCA | P,S 38 | XP_011524853.1 | |
XM_011526552.2 | 324 | Missense Mutation | CCA,TCA | P,S 38 | XP_011524854.1 | |
XM_011526553.2 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_011524855.1 | |
XM_011526554.2 | 324 | Intron | XP_011524856.1 | |||
XM_011526555.2 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_011524857.1 | |
XM_017026384.1 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_016881873.1 | |
XM_017026385.1 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_016881874.1 | |
XM_017026386.1 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_016881875.1 | |
XM_017026387.1 | 324 | Missense Mutation | CCA,TCA | P,S 113 | XP_016881876.1 |
Set Membership: |
DME Validated Inventoried |