Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615470 MIM: 604144 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CEP89 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CEP89 - centrosomal protein 89 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032816.4 | 2491 | Missense Mutation | CAT,CTT | H,L 779 | NP_116205.3 | |
XM_005259344.3 | 2491 | Missense Mutation | CAT,CTT | H,L 755 | XP_005259401.1 | |
XM_011527425.2 | 2491 | Missense Mutation | CAT,CTT | H,L 532 | XP_011525727.1 | |
XM_017027398.1 | 2491 | Intron | XP_016882887.1 |
SLC7A9 - solute carrier family 7 member 9 | ||||||
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There are no transcripts associated with this gene. |