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Search Thermo Fisher Scientific
CAGGGCTCGGCACCTAGAGGCTCTC[C/T]GGAGGCAGCTGCATGTGGAGCTGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610714 MIM: 600960 | ||||||||||||||||||||
Literature Links: |
PKN3 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 |
PKN3 - protein kinase N3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317926.1 | 814 | Missense Mutation | CGG,TGG | R,W 111 | NP_001304855.1 | |
NM_013355.4 | 814 | Missense Mutation | CGG,TGG | R,W 111 | NP_037487.2 | |
XM_005251946.3 | 814 | Missense Mutation | CGG,TGG | R,W 108 | XP_005252003.1 | |
XM_006717080.2 | 814 | Missense Mutation | CGG,TGG | R,W 118 | XP_006717143.1 | |
XM_017014649.1 | 814 | Missense Mutation | CGG,TGG | R,W 118 | XP_016870138.1 | |
XM_017014650.1 | 814 | UTR 5 | XP_016870139.1 |
SET - SET nuclear proto-oncogene | ||||||
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There are no transcripts associated with this gene. |