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- SNP ID:
- rs778179668
- Gene
-
CCT8MAP3K7CL - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.21: 29073424 - 29073424 on Build GRCh38
- Polymorphism:
- T/A, Transversion substitution
- Context Sequence [VIC/FAM]:
TGGAATCTTCTCTTCCCCCGGCCGC[T/A]GAGCCAGGGCAGCACGCTCAGCCCG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611110
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Literature Links: |
CCT8 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 |
| CCT8 - chaperonin containing TCP1 subunit 8 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001282907.1 | Intron | NP_001269836.1 | ||||
| NM_001282908.1 | Intron | NP_001269837.1 | ||||
| NM_001282909.1 | Intron | NP_001269838.1 | ||||
| NM_006585.3 | Intron | NP_006576.2 | ||||
| MAP3K7CL - MAP3K7 C-terminal like | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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