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GGATGGAGGGCAACCGGACTGGGGT[C/T]AGCAGGCTGTCCAGCCAGGTGGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147575 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C5orf56 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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C5orf56 - chromosome 5 open reading frame 56 | ||||||
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There are no transcripts associated with this gene. |
IRF1 - interferon regulatory factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002198.2 | 1041 | Silent Mutation | CTA,CTG | L,L 310 | NP_002189.1 | |
XM_011543378.2 | 1041 | Silent Mutation | CTA,CTG | L,L 269 | XP_011541680.1 | |
XM_011543379.2 | 1041 | Silent Mutation | CTA,CTG | L,L 226 | XP_011541681.1 |