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TCCCTGTGCTCCTCCGCCTCCACCG[C/T]CAGCCTCCAGTCCCCAAGGAGCACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf87 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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C11orf87 - chromosome 11 open reading frame 87 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207645.3 | 1012 | Missense Mutation | CCA,TCA | P,S 169 | NP_997528.2 | |
XM_011542817.2 | 1012 | Missense Mutation | CCA,TCA | P,S 316 | XP_011541119.1 | |
XM_011542818.2 | 1012 | Missense Mutation | CCA,TCA | P,S 169 | XP_011541120.1 |