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GAAACTAGGACTATGTACACCAGAA[A/G]CACTGTTTTGTTGTGATGTTACAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 610468 MIM: 613975 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFI44 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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IFI44 - interferon induced protein 44 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006417.4 | 1657 | Missense Mutation | ACA,GCA | T,A 99 | NP_006408.3 | |
XM_005270380.3 | 1657 | Missense Mutation | ACA,GCA | T,A 99 | XP_005270437.1 | |
XM_011540516.2 | 1657 | Missense Mutation | ACA,GCA | T,A 99 | XP_011538818.1 | |
XM_017000083.1 | 1657 | Missense Mutation | ACA,GCA | T,A 99 | XP_016855572.1 |
IFI44L - interferon induced protein 44 like | ||||||
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There are no transcripts associated with this gene. |