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GTGGCACGGGCATGGTTGGTGAGTA[C/T]GGAGCATGGTGAAGCATGATGGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 123930 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP2B6 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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CYP2B6 - cytochrome P450 family 2 subfamily B member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000767.4 | Intron | NP_000758.1 | ||||
XM_005258569.4 | Intron | XP_005258626.1 | ||||
XM_006723050.3 | Intron | XP_006723113.1 | ||||
XM_011526546.2 | Intron | XP_011524848.1 | ||||
XM_011526547.2 | Intron | XP_011524849.1 | ||||
XM_011526548.2 | Intron | XP_011524850.1 | ||||
XM_011526549.2 | Intron | XP_011524851.1 | ||||
XM_011526550.2 | Intron | XP_011524852.1 |