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TCCTTGATGTTCTCTTGGTCGAAAC[A/G]GAAGGGGTCGTAGACCTGCAGGTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611517 | ||||||||||||||||||||
Literature Links: |
CYP4F11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CYP4F11 - cytochrome P450 family 4 subfamily F member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128932.1 | 1788 | Missense Mutation | NP_001122404.1 | |||
NM_021187.3 | 1788 | Missense Mutation | NP_067010.3 |