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CAGCTGGGCGTGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTTGGGAGGCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606534 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP3A43 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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CYP3A43 - cytochrome P450 family 3 subfamily A member 43 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278921.1 | 314 | Missense Mutation | ATA,GTA | I,V 71 | NP_001265850.1 | |
NM_022820.4 | 314 | Intron | NP_073731.1 | |||
NM_057095.2 | 314 | Intron | NP_476436.1 | |||
NM_057096.3 | 314 | Intron | NP_476437.1 | |||
XM_017012542.1 | 314 | Intron | XP_016868031.1 | |||
XM_017012543.1 | 314 | Intron | XP_016868032.1 | |||
XM_017012544.1 | 314 | Intron | XP_016868033.1 | |||
XM_017012545.1 | 314 | Intron | XP_016868034.1 |