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AGGATGAAGATGGGACCTTGGAAAC[C/T]TGACAGTTTGCTGCAGCGGCCAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610999 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EPC1 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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EPC1 - enhancer of polycomb homolog 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272004.1 | 2697 | Silent Mutation | CAA,CAG | Q,Q 775 | NP_001258933.1 | |
NM_001272019.2 | 2697 | Silent Mutation | CAA,CAG | Q,Q 704 | NP_001258948.1 | |
NM_001282391.1 | 2697 | Silent Mutation | CAA,CAG | Q,Q 725 | NP_001269320.1 | |
NM_025209.3 | 2697 | Silent Mutation | CAA,CAG | Q,Q 798 | NP_079485.1 | |
XM_006717510.1 | 2697 | Silent Mutation | CAA,CAG | Q,Q 748 | XP_006717573.1 |