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TGATGTTGTCCATCCTGCAGCAAAG[A/G]CTTTGGTAGACATTGCCAAATCCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605140 | ||||||||||||||||||||
Literature Links: |
CCT7 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 |
CCT7 - chaperonin containing TCP1 subunit 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009570.2 | 375 | Intron | NP_001009570.1 | |||
NM_001166284.1 | 375 | Intron | NP_001159756.1 | |||
NM_001166285.1 | 375 | Missense Mutation | ACT,GCT | T,A 34 | NP_001159757.1 | |
NM_006429.3 | 375 | Missense Mutation | ACT,GCT | T,A 78 | NP_006420.1 | |
XM_011532478.2 | 375 | Missense Mutation | ACT,GCT | T,A 34 | XP_011530780.1 | |
XM_011532479.1 | 375 | Missense Mutation | ACT,GCT | T,A 34 | XP_011530781.1 |
PRADC1 - protease associated domain containing 1 | ||||||
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There are no transcripts associated with this gene. |