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AATAGAAACTTTACTCTTAAATACA[A/G]CACCAAAAATTATTGATGAGCAACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
42 submissions
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Phenotype: |
MIM: 613975 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFI44L 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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IFI44L - interferon induced protein 44 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006820.3 | 348 | Missense Mutation | ACA,GCA | T,A 104 | NP_006811.2 | |
XM_005270391.3 | 348 | Intron | XP_005270448.1 | |||
XM_005270392.4 | 348 | Intron | XP_005270449.1 | |||
XM_005270393.4 | 348 | Intron | XP_005270450.1 | |||
XM_006710304.3 | 348 | Intron | XP_006710367.1 | |||
XM_011540539.2 | 348 | Missense Mutation | ACA,GCA | T,A 104 | XP_011538841.1 | |
XM_017000120.1 | 348 | Intron | XP_016855609.1 |