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CACGCTGAATTCCACCCGTTGCAGC[A/G]GGATAGCCAGGAAGAGAAAGACCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 108330 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP1A1 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | 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 | 1620 | Missense Mutation | CCG,CTG | P,L 474 | NP_000490.1 | |
NM_001319216.1 | 1620 | Missense Mutation | CCG,CTG | P,L 445 | NP_001306145.1 | |
NM_001319217.1 | 1620 | Missense Mutation | CCG,CTG | P,L 474 | NP_001306146.1 | |
XM_017021953.1 | 1620 | Missense Mutation | CCG,CTG | P,L 446 | XP_016877442.1 |