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CAATTCATAAAATTAAAATAATAAC[A/C]GCTCAACTTAAGCAAGCGCTTTTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600009 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFI27 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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IFI27 - interferon alpha inducible protein 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130080.2 | Intron | NP_001123552.1 | ||||
NM_001288952.1 | Intron | NP_001275881.1 | ||||
NM_001288954.1 | Intron | NP_001275883.1 | ||||
NM_001288956.1 | Intron | NP_001275885.1 | ||||
NM_001288957.1 | Intron | NP_001275886.1 | ||||
NM_001288958.1 | Intron | NP_001275887.1 | ||||
NM_001288959.1 | Intron | NP_001275888.1 | ||||
NM_001288960.1 | Intron | NP_001275889.1 | ||||
NM_001288995.1 | Intron | NP_001275924.1 | ||||
NM_005532.4 | Intron | NP_005523.3 |