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AACATTTGCAAGAAGCTTTCAAATC[A/C]CTTCCGCTATAGAATGGAGTGTCCA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147690 | |||||||||||||||||||||||
Literature Links: |
IFIT1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
IFIT1 - interferon induced protein with tetratricopeptide repeats 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270927.1 | 668 | Missense Mutation | CAC,CCC | H,P 131 | NP_001257856.1 | |
NM_001270928.1 | 668 | Missense Mutation | CAC,CCC | H,P 100 | NP_001257857.1 | |
NM_001270929.1 | 668 | Missense Mutation | CAC,CCC | H,P 100 | NP_001257858.1 | |
NM_001270930.1 | 668 | Missense Mutation | CAC,CCC | H,P 100 | NP_001257859.1 | |
NM_001548.4 | 668 | Missense Mutation | CAC,CCC | H,P 131 | NP_001539.3 |