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CAAAACAAAGGGGATTTGGTGATGG[A/T]GGCTTTGTTAGAAGGAATACAAAAT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614484 MIM: 614724 | |||||||||||||||||||||||
Literature Links: |
ANAPC13 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
ANAPC13 - anaphase promoting complex subunit 13 | ||||||
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There are no transcripts associated with this gene. |
CEP63 - centrosomal protein 63 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042383.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | NP_001035842.1 | |
NM_001042384.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | NP_001035843.1 | |
NM_001042400.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | NP_001035859.1 | |
NM_025180.3 | 59 | Missense Mutation | GAG,GTG | E,V 2 | NP_079456.2 | |
XM_005247795.4 | 59 | Silent Mutation | GGA,GGT | G,G 12 | XP_005247852.1 | |
XM_005247797.3 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_005247854.1 | |
XM_005247799.3 | 59 | UTR 5 | XP_005247856.1 | |||
XM_006713760.3 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_006713823.1 | |
XM_011513194.2 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_011511496.1 | |
XM_011513197.2 | 59 | Intron | XP_011511499.1 | |||
XM_017007244.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862733.1 | |
XM_017007245.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862734.1 | |
XM_017007246.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862735.1 | |
XM_017007247.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862736.1 | |
XM_017007248.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862737.1 | |
XM_017007249.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862738.1 | |
XM_017007250.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862739.1 | |
XM_017007251.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862740.1 | |
XM_017007252.1 | 59 | UTR 5 | XP_016862741.1 | |||
XM_017007253.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862742.1 | |
XM_017007254.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862743.1 | |
XM_017007255.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862744.1 | |
XM_017007256.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862745.1 | |
XM_017007257.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862746.1 | |
XM_017007258.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862747.1 | |
XM_017007259.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862748.1 | |
XM_017007260.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862749.1 | |
XM_017007261.1 | 59 | Silent Mutation | GGA,GGT | G,G 12 | XP_016862750.1 | |
XM_017007262.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862751.1 | |
XM_017007263.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862752.1 | |
XM_017007264.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862753.1 | |
XM_017007265.1 | 59 | Silent Mutation | GGA,GGT | G,G 19 | XP_016862754.1 | |
XM_017007266.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862755.1 | |
XM_017007267.1 | 59 | Missense Mutation | GAG,GTG | E,V 2 | XP_016862756.1 | |
XM_017007268.1 | 59 | UTR 5 | XP_016862757.1 | |||
XM_017007269.1 | 59 | UTR 5 | XP_016862758.1 |