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TGGGGGGGACCATGGCTGACGTTTT[C/T]CCGGGCAACGACTCCACGGCGTCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 176960 | ||||||||||||||||||||
Literature Links: |
PRKCA 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 |
PRKCA - protein kinase C alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002737.2 | 59 | Silent Mutation | TTC,TTT | F,F 5 | NP_002728.1 | |
XM_017024836.1 | 59 | Silent Mutation | TTC,TTT | F,F 5 | XP_016880325.1 | |
XM_017024837.1 | 59 | Intron | XP_016880326.1 | |||
XM_017024838.1 | 59 | Intron | XP_016880327.1 | |||
XM_017024839.1 | 59 | Intron | XP_016880328.1 | |||
XM_017024840.1 | 59 | Intron | XP_016880329.1 | |||
XM_017024841.1 | 59 | Silent Mutation | TTC,TTT | F,F 5 | XP_016880330.1 |