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ATCTTGCCCCGACCCAGGCCTCTCA[A/G]AGGGGGAAGGTCTCCCTCTTTCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
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Literature Links: |
MIR5585 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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MIR5585 - microRNA 5585 | ||||||
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There are no transcripts associated with this gene. |
TMEM39B - transmembrane protein 39B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319677.1 | 862 | Silent Mutation | CAA,CAG | Q,Q 21 | NP_001306606.1 | |
NM_001319678.1 | 862 | Intron | NP_001306607.1 | |||
NM_001319679.1 | 862 | Intron | NP_001306608.1 | |||
NM_018056.3 | 862 | Silent Mutation | CAA,CAG | Q,Q 148 | NP_060526.2 | |
XM_005270988.2 | 862 | Silent Mutation | CAA,CAG | Q,Q 21 | XP_005271045.1 | |
XM_006710724.1 | 862 | Silent Mutation | CAA,CAG | Q,Q 148 | XP_006710787.1 | |
XM_006710725.3 | 862 | Silent Mutation | CAA,CAG | Q,Q 148 | XP_006710788.1 | |
XM_011541681.2 | 862 | Silent Mutation | CAA,CAG | Q,Q 148 | XP_011539983.1 | |
XM_011541683.1 | 862 | Silent Mutation | CAA,CAG | Q,Q 21 | XP_011539985.1 | |
XM_011541684.2 | 862 | Intron | XP_011539986.1 | |||
XM_017001595.1 | 862 | Silent Mutation | CAA,CAG | Q,Q 33 | XP_016857084.1 |