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TCGGAGAAGGCCAAAGAGCAGCAGG[C/T]GGAGGCAGAGCTCCGGAAGCTAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC63 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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CCDC63 - coiled-coil domain containing 63 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286243.1 | 217 | UTR 5 | NP_001273172.1 | |||
NM_001286244.1 | 217 | Intron | NP_001273173.1 | |||
NM_152591.2 | 217 | Missense Mutation | GCG,GTG | A,V 27 | NP_689804.1 | |
XM_006719262.1 | 217 | Missense Mutation | GCG,GTG | A,V 27 | XP_006719325.1 | |
XM_006719263.2 | 217 | Missense Mutation | GCG,GTG | A,V 27 | XP_006719326.1 | |
XM_011537999.1 | 217 | Missense Mutation | GCG,GTG | A,V 27 | XP_011536301.1 | |
XM_011538001.2 | 217 | Missense Mutation | GCG,GTG | A,V 27 | XP_011536303.1 |