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- SNP ID:
- rs763866438
- Gene
-
CEP192 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.18: 13100587 - 13100587 on Build GRCh38
- Polymorphism:
- G/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TCTAATGCTTTATTCTTAGCCATAA[G/C]TTGGTGATAAATATAAATTTCCTCC
Genomic Map
Back To TopAssay 상세 정보
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616426
|
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Literature Links: |
CEP192 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 |
| CEP192 - centrosomal protein 192 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_032142.3 | Intron | NP_115518.3 | ||||
| XM_005258107.3 | Intron | XP_005258164.1 | ||||
| XM_005258109.3 | Intron | XP_005258166.1 | ||||
| XM_005258110.1 | Intron | XP_005258167.1 | ||||
| XM_006722326.3 | Intron | XP_006722389.1 | ||||
| XM_006722327.3 | Intron | XP_006722390.1 | ||||
| XM_006722330.3 | Intron | XP_006722393.1 | ||||
| XM_011525673.2 | Intron | XP_011523975.1 | ||||
| XM_011525675.2 | Intron | XP_011523977.1 | ||||
| XM_017025803.1 | Intron | XP_016881292.1 | ||||
| XM_017025804.1 | Intron | XP_016881293.1 | ||||
| XM_017025805.1 | Intron | XP_016881294.1 | ||||
| XM_017025806.1 | Intron | XP_016881295.1 | ||||
| XM_017025807.1 | Intron | XP_016881296.1 | ||||
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