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GGCTGCTGGTGATCACGGAGGGCTC[C/T]GGGCTCTGTATGGGCAGGAGGAGGC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609843 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCP1B 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)
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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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DCP1B - decapping mRNA 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319292.1 | 1926 | Intron | NP_001306221.1 | |||
NM_152640.4 | 1926 | Silent Mutation | CCA,CCG | P,P 567 | NP_689853.3 | |
XM_011520927.2 | 1926 | Silent Mutation | CCA,CCG | P,P 465 | XP_011519229.1 |
Set Membership: |
HapMap |