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GCTGGTTGTGGGCTCCTGGCTACTC[G/T]CCCGCATCCTGGCTTGGACCTATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611485 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP4F12 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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CYP4F12 - cytochrome P450 family 4 subfamily F member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023944.3 | 208 | Intron | NP_076433.3 | |||
XM_006722850.3 | 208 | UTR 5 | XP_006722913.1 | |||
XM_011528202.2 | 208 | Intron | XP_011526504.1 | |||
XM_011528203.2 | 208 | Intron | XP_011526505.1 | |||
XM_011528204.2 | 208 | Intron | XP_011526506.1 | |||
XM_011528205.2 | 208 | Intron | XP_011526507.1 | |||
XM_011528207.2 | 208 | Intron | XP_011526509.1 | |||
XM_011528208.2 | 208 | Intron | XP_011526510.1 | |||
XM_017027172.1 | 208 | Missense Mutation | GCC,TCC | A,S 32 | XP_016882661.1 |