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Search Thermo Fisher Scientific
TGTAACAGAACTTATAATGGAATCC[A/G]ATGTAGAGCTCATAGCAAAAAATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CEP44 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
CEP44 - centrosomal protein 44 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040157.2 | 522 | Missense Mutation | AAT,GAT | N,D 62 | NP_001035247.1 | |
NM_001145314.1 | 522 | Missense Mutation | AAT,GAT | N,D 62 | NP_001138786.1 | |
XM_011532285.2 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_011530587.1 | |
XM_011532286.2 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_011530588.1 | |
XM_011532287.2 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_011530589.1 | |
XM_017008654.1 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_016864143.1 | |
XM_017008655.1 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_016864144.1 | |
XM_017008656.1 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_016864145.1 | |
XM_017008657.1 | 522 | Missense Mutation | AAT,GAT | N,D 62 | XP_016864146.1 | |
XM_017008658.1 | 522 | UTR 5 | XP_016864147.1 | |||
XM_017008659.1 | 522 | UTR 5 | XP_016864148.1 | |||
XM_017008660.1 | 522 | UTR 5 | XP_016864149.1 |