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TCACCATGGACAGCATAAGCACAGC[C/T]ATCTTACTCCTGCTCCTGGCTCTCG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CYP2F1 - cytochrome P450 family 2 subfamily F member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000774.4 | 233 | Silent Mutation | GCC,GCT | A,A 7 | NP_000765.2 | |
XM_011526551.2 | 233 | Silent Mutation | GCC,GCT | A,A 7 | XP_011524853.1 | |
XM_011526552.2 | 233 | Silent Mutation | GCC,GCT | A,A 7 | XP_011524854.1 | |
XM_011526553.2 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_011524855.1 | |
XM_011526554.2 | 233 | Intron | XP_011524856.1 | |||
XM_011526555.2 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_011524857.1 | |
XM_017026384.1 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_016881873.1 | |
XM_017026385.1 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_016881874.1 | |
XM_017026386.1 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_016881875.1 | |
XM_017026387.1 | 233 | Silent Mutation | GCC,GCT | A,A 82 | XP_016881876.1 |