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CTCATCACTAACGAATCCCAGCCAC[C/T]GGCACCTGCTGCTGCTTGCGGATCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612915 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MED20 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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MED20 - mediator complex subunit 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305455.1 | 867 | Silent Mutation | CCA,CCG | P,P 145 | NP_001292384.1 | |
NM_001305456.1 | 867 | Silent Mutation | CCA,CCG | P,P 145 | NP_001292385.1 | |
NM_001305457.1 | 867 | UTR 3 | NP_001292386.1 | |||
NM_004275.4 | 867 | Silent Mutation | CCA,CCG | P,P 207 | NP_004266.2 |