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AGCAAAAATAAAGATAATTGATTGG[A/G]CCATGAGCTCCAGATCAGACAGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605340 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP3A7 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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CYP3A7 - cytochrome P450 family 3 subfamily A member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000765.4 | 997 | Missense Mutation | GCC,GTC | A,V 297 | NP_000756.3 |
CYP3A7-CYP3A51P - CYP3A7-CYP3A51P readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256497.2 | 997 | Missense Mutation | GCC,GTC | A,V 297 | NP_001243426.2 |
ZSCAN25 - zinc finger and SCAN domain containing 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145115.2 | 997 | Intron | NP_660090.2 | |||
XM_005250194.2 | 997 | Intron | XP_005250251.1 | |||
XM_011515905.2 | 997 | Intron | XP_011514207.1 | |||
XM_011515906.2 | 997 | Intron | XP_011514208.1 | |||
XM_011515907.2 | 997 | Intron | XP_011514209.1 | |||
XM_011515908.2 | 997 | Intron | XP_011514210.1 | |||
XM_011515909.2 | 997 | Intron | XP_011514211.1 | |||
XM_011515910.2 | 997 | Intron | XP_011514212.1 | |||
XM_017011824.1 | 997 | Intron | XP_016867313.1 | |||
XM_017011825.1 | 997 | Intron | XP_016867314.1 | |||
XM_017011826.1 | 997 | Intron | XP_016867315.1 | |||
XM_017011827.1 | 997 | Intron | XP_016867316.1 |