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GTGCCTGGTGCTCTGGGCCCTCCAG[C/T]GGGGGCCCCACTGCGGGCGTGGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601206 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR4491 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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MIR4491 - microRNA 4491 | ||||||
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There are no transcripts associated with this gene. |
POU2AF1 - POU class 2 associating factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006235.2 | 2448 | Silent Mutation | NP_006226.2 | |||
XM_005271593.1 | 2448 | Silent Mutation | XP_005271650.1 | |||
XM_005271594.3 | 2448 | Silent Mutation | XP_005271651.1 | |||
XM_006718859.1 | 2448 | Silent Mutation | XP_006718922.1 | |||
XM_006718860.3 | 2448 | UTR 3 | XP_006718923.1 | |||
XM_017017932.1 | 2448 | UTR 3 | XP_016873421.1 |