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GGCTGTACCTTCTGCCTTGATATGT[A/C]GTCAGTTCTTCCTGAAGGATGGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CEP112 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 |
CEP112 - centrosomal protein 112 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037325.2 | 3097 | Silent Mutation | ACG,ACT | T,T 205 | NP_001032402.1 | |
NM_001199165.2 | 3097 | Silent Mutation | ACG,ACT | T,T 949 | NP_001186094.1 | |
NM_001302891.1 | 3097 | Silent Mutation | ACG,ACT | T,T 907 | NP_001289820.1 | |
XM_005257119.4 | 3097 | Silent Mutation | ACG,ACT | T,T 950 | XP_005257176.1 | |
XM_005257125.3 | 3097 | Silent Mutation | ACG,ACT | T,T 642 | XP_005257182.1 | |
XM_005257126.4 | 3097 | Silent Mutation | ACG,ACT | T,T 541 | XP_005257183.1 | |
XM_006721740.2 | 3097 | Silent Mutation | ACG,ACT | T,T 950 | XP_006721803.1 | |
XM_006721744.3 | 3097 | Intron | XP_006721807.1 | |||
XM_011524461.2 | 3097 | Silent Mutation | ACG,ACT | T,T 949 | XP_011522763.1 | |
XM_011524462.2 | 3097 | Intron | XP_011522764.1 | |||
XM_011524463.2 | 3097 | Intron | XP_011522765.1 | |||
XM_011524464.2 | 3097 | Silent Mutation | ACG,ACT | T,T 879 | XP_011522766.1 | |
XM_011524465.2 | 3097 | Silent Mutation | ACG,ACT | T,T 719 | XP_011522767.1 | |
XM_011524466.2 | 3097 | Silent Mutation | ACG,ACT | T,T 597 | XP_011522768.1 | |
XM_011524467.2 | 3097 | Silent Mutation | ACG,ACT | T,T 544 | XP_011522769.1 | |
XM_017024302.1 | 3097 | Silent Mutation | ACG,ACT | T,T 907 | XP_016879791.1 | |
XM_017024303.1 | 3097 | Intron | XP_016879792.1 |