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ACCATGGCTGACGTTTTCCCGGGCA[A/G]CGACTCCACGGCGTCTCAGGACGTG
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 67 | Missense Mutation | AAC,AGC | N,S 8 | NP_002728.1 | |
XM_017024836.1 | 67 | Missense Mutation | AAC,AGC | N,S 8 | XP_016880325.1 | |
XM_017024837.1 | 67 | Intron | XP_016880326.1 | |||
XM_017024838.1 | 67 | Intron | XP_016880327.1 | |||
XM_017024839.1 | 67 | Intron | XP_016880328.1 | |||
XM_017024840.1 | 67 | Intron | XP_016880329.1 | |||
XM_017024841.1 | 67 | Missense Mutation | AAC,AGC | N,S 8 | XP_016880330.1 |