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ACATCGCGACGCTGCTCAAAACCTC[A/G]CTCCGGAAAGGGGACACCTGGTAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604731 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR6125 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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MIR6125 - microRNA 6125 | ||||||
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There are no transcripts associated with this gene. |
USP15 - ubiquitin specific peptidase 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252078.1 | 142 | Silent Mutation | TCA,TCG | S,S 23 | NP_001239007.1 | |
NM_001252079.1 | 142 | Silent Mutation | TCA,TCG | S,S 23 | NP_001239008.1 | |
NM_006313.2 | 142 | Silent Mutation | TCA,TCG | S,S 23 | NP_006304.1 | |
XM_005269261.2 | 142 | Intron | XP_005269318.1 | |||
XM_006719718.3 | 142 | Silent Mutation | TCA,TCG | S,S 23 | XP_006719781.1 | |
XM_017020284.1 | 142 | Intron | XP_016875773.1 | |||
XM_017020285.1 | 142 | UTR 5 | XP_016875774.1 |