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ATGCCTTCAACACATTGTACACCAA[C/T]GCCACAATAGCCCTGGAAAGCACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601647 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPP2R5E 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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PPP2R5E - protein phosphatase 2 regulatory subunit B'epsilon | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282179.1 | 1805 | Silent Mutation | GCA,GCG | A,A 405 | NP_001269108.1 | |
NM_001282180.1 | 1805 | Silent Mutation | GCA,GCG | A,A 405 | NP_001269109.1 | |
NM_001282181.1 | 1805 | Silent Mutation | GCA,GCG | A,A 329 | NP_001269110.1 | |
NM_001282182.1 | 1805 | Silent Mutation | GCA,GCG | A,A 329 | NP_001269111.1 | |
NM_006246.3 | 1805 | Silent Mutation | GCA,GCG | A,A 405 | NP_006237.1 |