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CTCTGCAGCCTATCAACATCTCTGT[A/G]CATCAGTAGATTACTTGAGCCTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CEP57L1 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CEP57L1 - centrosomal protein 57 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083535.1 | Intron | NP_001077004.1 | ||||
NM_001271852.1 | Intron | NP_001258781.1 | ||||
NM_001271853.1 | Intron | NP_001258782.1 | ||||
NM_173830.4 | Intron | NP_776191.1 | ||||
XM_005266935.4 | Intron | XP_005266992.3 | ||||
XM_005266936.4 | Intron | XP_005266993.3 | ||||
XM_005266937.4 | Intron | XP_005266994.3 | ||||
XM_005266938.4 | Intron | XP_005266995.3 | ||||
XM_006715462.3 | Intron | XP_006715525.1 | ||||
XM_011535759.2 | Intron | XP_011534061.1 | ||||
XM_011535762.2 | Intron | XP_011534064.1 | ||||
XM_011535763.2 | Intron | XP_011534065.2 | ||||
XM_017010764.1 | Intron | XP_016866253.1 | ||||
XM_017010765.1 | Intron | XP_016866254.1 | ||||
XM_017010767.1 | Intron | XP_016866256.1 | ||||
XM_017010768.1 | Intron | XP_016866257.1 | ||||
XM_017010769.1 | Intron | XP_016866258.1 | ||||
XM_017010770.1 | Intron | XP_016866259.1 | ||||
XM_017010771.1 | Intron | XP_016866260.1 | ||||
XM_017010772.1 | Intron | XP_016866261.1 |