Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAAGGATGGAGATGTGACTGTAACT[A/C]ATGATGGGGCCACCATCTTAAGCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610150 | ||||||||||||||||||||
Literature Links: |
CCT5 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 |
CCT5 - chaperonin containing TCP1 subunit 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306153.1 | 466 | Missense Mutation | AAT,CAT | N,H 51 | NP_001293082.1 | |
NM_001306154.1 | 466 | Intron | NP_001293083.1 | |||
NM_001306155.1 | 466 | Intron | NP_001293084.1 | |||
NM_001306156.1 | 466 | Missense Mutation | AAT,CAT | N,H 34 | NP_001293085.1 | |
NM_012073.4 | 466 | Missense Mutation | AAT,CAT | N,H 72 | NP_036205.1 |
FAM173B - family with sequence similarity 173 member B | ||||||
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There are no transcripts associated with this gene. |