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CCACACCCCCCAAGGCAACAGCAGT[C/T]GCCCCAAACAGCCACTTCCATGGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604840 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FKBP8 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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FKBP8 - FK506 binding protein 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308373.1 | 1379 | Silent Mutation | GCA,GCG | A,A 394 | NP_001295302.1 | |
NM_012181.4 | 1379 | Silent Mutation | GCA,GCG | A,A 395 | NP_036313.3 | |
XM_011527863.1 | 1379 | Silent Mutation | GCA,GCG | A,A 395 | XP_011526165.1 | |
XM_011527864.1 | 1379 | UTR 3 | XP_011526166.1 |