Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCCTTTTGGGAAACCTTCTGCAG[A/G]TGGATAGAAGAGGCCTACTCAAATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 123930 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP2B6 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
CYP2B6*11A,c.136A>G CYP2B6*11A,g.136A>G CYP2B6*11B,c.136A>G CYP2B6*11B,g.136A>G | ||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU) - Not Available | ||||||
EAS
|
African American
|
YRI (Yoruba) - Not Available | ||||||
SAS
|
Japanese
|
CHB (Han Chinese) - Not Available | ||||||
AFR
|
Chinese
|
JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
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 | 239 | Missense Mutation | ATG,GTG | M,V 46 | NP_000758.1 | |
XM_005258569.4 | 239 | Missense Mutation | ATG,GTG | M,V 46 | XP_005258626.1 | |
XM_006723050.3 | 239 | Missense Mutation | ATG,GTG | M,V 46 | XP_006723113.1 | |
XM_011526546.2 | 239 | Missense Mutation | ATG,GTG | M,V 46 | XP_011524848.1 | |
XM_011526547.2 | 239 | Intron | XP_011524849.1 | |||
XM_011526548.2 | 239 | Missense Mutation | ATG,GTG | M,V 46 | XP_011524850.1 | |
XM_011526549.2 | 239 | Intron | XP_011524851.1 | |||
XM_011526550.2 | 239 | Intron | XP_011524852.1 |
Set Membership: |
DME Validated Inventoried |