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CGTGGCTATGTTCGTGTCCGATTTC[C/G]GCAAAGAGTTCTACGAGGTGGTCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603465 MIM: 601754 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC45 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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CDC45 - cell division cycle 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178010.2 | 162 | Missense Mutation | CGC,GGC | R,G 7 | NP_001171481.1 | |
NM_001178011.2 | 162 | Missense Mutation | CGC,GGC | R,G 7 | NP_001171482.1 | |
NM_003504.4 | 162 | Missense Mutation | CGC,GGC | R,G 7 | NP_003495.1 | |
XM_005261285.2 | 162 | Missense Mutation | CGC,GGC | R,G 7 | XP_005261342.1 | |
XM_005261286.3 | 162 | Missense Mutation | CGC,GGC | R,G 7 | XP_005261343.1 | |
XM_011530415.1 | 162 | Missense Mutation | CGC,GGC | R,G 7 | XP_011528717.1 | |
XM_011530416.1 | 162 | Intron | XP_011528718.1 | |||
XM_011530417.2 | 162 | Missense Mutation | CGC,GGC | R,G 7 | XP_011528719.1 | |
XM_011530418.2 | 162 | Missense Mutation | CGC,GGC | R,G 7 | XP_011528720.1 | |
XM_017028966.1 | 162 | Intron | XP_016884455.1 | |||
XM_017028967.1 | 162 | Intron | XP_016884456.1 |
UFD1L - ubiquitin fusion degradation 1 like (yeast) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001035247.2 | 162 | Intron | NP_001030324.2 | |||
NM_005659.6 | 162 | Intron | NP_005650.2 | |||
XM_011530361.2 | 162 | Intron | XP_011528663.1 |