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AAACAACCTGGTGAAGTCTCGCAAG[A/G]CCCAGCAAACTTGTTTACATTCCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607218 MIM: 610032 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IRF5 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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IRF5 - interferon regulatory factor 5 | ||||||
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There are no transcripts associated with this gene. |
TNPO3 - transportin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001191028.2 | 3144 | Missense Mutation | GCC,GTC | A,V 850 | NP_001177957.2 | |
NM_012470.3 | 3144 | Missense Mutation | GCC,GTC | A,V 914 | NP_036602.1 | |
XM_011515989.2 | 3144 | Missense Mutation | GCC,GTC | A,V 848 | XP_011514291.1 |