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AGGTGGTGGCGAGGGTCACACGCTG[C/T]CTGGGCCAGGACTCGGTGACTTCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CEP170B 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 |
CEP170B - centrosomal protein 170B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001112726.2 | Intron | NP_001106197.1 | ||||
NM_015005.2 | Intron | NP_055820.2 | ||||
XM_005267550.3 | Intron | XP_005267607.1 | ||||
XM_011536665.2 | Intron | XP_011534967.1 | ||||
XM_011536666.2 | Intron | XP_011534968.1 | ||||
XM_011536667.2 | Intron | XP_011534969.1 | ||||
XM_017021227.1 | Intron | XP_016876716.1 | ||||
XM_017021228.1 | Intron | XP_016876717.1 | ||||
XM_017021229.1 | Intron | XP_016876718.1 | ||||
XM_017021230.1 | Intron | XP_016876719.1 |