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CCTGCACAACGTCAGCCAGAACATC[A/G]CGGCCGAGACCCGGGCTGAGGACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
MIM: 616690 MIM: 601883 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CEP104 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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CEP104 - centrosomal protein 104 | ||||||
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There are no transcripts associated with this gene. |
DFFB - DNA fragmentation factor subunit beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282669.1 | 728 | Missense Mutation | ACG,GCG | T,A 155 | NP_001269598.1 | |
NM_001320132.1 | 728 | Missense Mutation | ACG,GCG | T,A 82 | NP_001307061.1 | |
NM_001320136.1 | 728 | Missense Mutation | ACG,GCG | T,A 67 | NP_001307065.1 | |
NM_004402.3 | 728 | Missense Mutation | ACG,GCG | T,A 131 | NP_004393.1 | |
XM_011540865.2 | 728 | Missense Mutation | ACG,GCG | T,A 155 | XP_011539167.1 | |
XM_017000498.1 | 728 | Intron | XP_016855987.1 | |||
XM_017000499.1 | 728 | Missense Mutation | ACG,GCG | T,A 155 | XP_016855988.1 | |
XM_017000500.1 | 728 | Missense Mutation | ACG,GCG | T,A 131 | XP_016855989.1 |