Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
47 submissions
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Phenotype: |
MIM: 616876 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC18 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
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CEPH (CEU)
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EAS
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African American
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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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CCDC18 - coiled-coil domain containing 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306076.1 | Intron | NP_001293005.1 | ||||
NM_206886.4 | Intron | NP_996769.3 | ||||
XM_011541361.2 | Intron | XP_011539663.2 | ||||
XM_011541372.2 | Intron | XP_011539674.2 | ||||
XM_017001154.1 | Intron | XP_016856643.1 | ||||
XM_017001155.1 | Intron | XP_016856644.1 | ||||
XM_017001156.1 | Intron | XP_016856645.1 | ||||
XM_017001157.1 | Intron | XP_016856646.1 | ||||
XM_017001158.1 | Intron | XP_016856647.1 | ||||
XM_017001159.1 | Intron | XP_016856648.1 | ||||
XM_017001160.1 | Intron | XP_016856649.1 | ||||
XM_017001161.1 | Intron | XP_016856650.1 | ||||
XM_017001162.1 | Intron | XP_016856651.1 | ||||
XM_017001163.1 | Intron | XP_016856652.1 | ||||
XM_017001164.1 | Intron | XP_016856653.1 | ||||
XM_017001165.1 | Intron | XP_016856654.1 | ||||
XM_017001166.1 | Intron | XP_016856655.1 | ||||
XM_017001167.1 | Intron | XP_016856656.1 | ||||
XM_017001168.1 | Intron | XP_016856657.1 | ||||
XM_017001169.1 | Intron | XP_016856658.1 | ||||
XM_017001170.1 | Intron | XP_016856659.1 | ||||
XM_017001171.1 | Intron | XP_016856660.1 |
TMED5 - transmembrane p24 trafficking protein 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167830.1 | Intron | NP_001161302.1 | ||||
NM_016040.4 | Intron | NP_057124.3 |
Set Membership: |
HapMap Validated |