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TGGCTAATTTTTTGTACTTTTAGTA[A/G]AGACTTTGCCATGTTGCCCAGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607218 | ||||||||||||||||||||
Literature Links: |
IRF5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
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 |
IRF5 - interferon regulatory factor 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098627.3 | Intron | NP_001092097.2 | ||||
NM_001098629.2 | Intron | NP_001092099.1 | ||||
NM_001098630.2 | Intron | NP_001092100.1 | ||||
NM_001242452.2 | Intron | NP_001229381.1 | ||||
NM_032643.4 | Intron | NP_116032.1 | ||||
XM_005250317.3 | Intron | XP_005250374.1 | ||||
XM_006715974.2 | Intron | XP_006716037.1 | ||||
XM_011516158.2 | Intron | XP_011514460.1 | ||||
XM_011516159.2 | Intron | XP_011514461.1 | ||||
XM_011516160.1 | Intron | XP_011514462.1 | ||||
XM_011516161.1 | Intron | XP_011514463.1 | ||||
XM_011516162.1 | Intron | XP_011514464.1 | ||||
XM_011516163.2 | Intron | XP_011514465.1 | ||||
XM_011516164.1 | Intron | XP_011514466.1 |