Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTCCTGGTTCAGCGCCACCCTAAC[A/T]CCCATGACCGCCTCCCACCAGGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 123930 | ||||||||||||||||||||||||||||||||
Literature Links: |
CYP2B6 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
CYP2B6*17A,c.76A>T CYP2B6*17A,g.76A>T CYP2B6*17B,c.76A>T CYP2B6*17B,g.76A>T | ||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
|
YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
|
CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
|
JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
CYP2B6 - cytochrome P450 family 2 subfamily B member 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000767.4 | 179 | Missense Mutation | ACC,TCC | T,S 26 | NP_000758.1 | |
XM_005258569.4 | 179 | Missense Mutation | ACC,TCC | T,S 26 | XP_005258626.1 | |
XM_006723050.3 | 179 | Missense Mutation | ACC,TCC | T,S 26 | XP_006723113.1 | |
XM_011526546.2 | 179 | Missense Mutation | ACC,TCC | T,S 26 | XP_011524848.1 | |
XM_011526547.2 | 179 | Intron | XP_011524849.1 | |||
XM_011526548.2 | 179 | Missense Mutation | ACC,TCC | T,S 26 | XP_011524850.1 | |
XM_011526549.2 | 179 | Intron | XP_011524851.1 | |||
XM_011526550.2 | 179 | Intron | XP_011524852.1 |
Set Membership: |
DME Validated Inventoried |