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ATGCTTCATGGTTAGCCCATAGATG[C/G]GGGTCATGTCCACCTTCACGCCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 108330 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP1A1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
CYP1A1*11,g.2546C>G | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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CYP1A1 - cytochrome P450 family 1 subfamily A member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000499.4 | 1674 | Missense Mutation | CCC,CGC | P,R 492 | NP_000490.1 | |
NM_001319216.1 | 1674 | Missense Mutation | CCC,CGC | P,R 463 | NP_001306145.1 | |
NM_001319217.1 | 1674 | Missense Mutation | CCC,CGC | P,R 492 | NP_001306146.1 | |
XM_017021953.1 | 1674 | Missense Mutation | CCC,CGC | P,R 464 | XP_016877442.1 |