Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACTTTTTTGCCTGATTCTTTCAGC[A/G]TCAACTGGCACTGGCTTCTGTGGGT
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)
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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 | 1818 | 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 | 1818 | Missense Mutation | CGC,TGC | R,C 368 | NP_001078955.1 | |
NM_001093726.1 | 1818 | Missense Mutation | CGC,TGC | R,C 398 | NP_001087195.1 | |
NM_005410.2 | 1818 | Missense Mutation | CGC,TGC | R,C 368 | NP_005401.3 |