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TGGAAACTTCTGTACCTGTGTCAAC[A/G]GTGCATCTTATCTAATACTATATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601484 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC152 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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CCDC152 - coiled-coil domain containing 152 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134848.1 | 3035 | UTR 3 | NP_001128320.1 |
SEPP1 - selenoprotein P, plasma, 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085486.1 | 3035 | Intron | NP_001078955.1 | |||
NM_001093726.1 | 3035 | Intron | NP_001087195.1 | |||
NM_005410.2 | 3035 | Intron | NP_005401.3 |