Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCATGCAGGTGTCTTCGTCCTCCT[C/G]CTCACACTCCCTGTCAGCCTCCGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605213 | ||||||||||||||||||||
Literature Links: |
PDPK1 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 |
PDPK1 - 3-phosphoinositide dependent protein kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001261816.1 | 889 | Missense Mutation | TCC,TGC | S,C 393 | NP_001248745.1 | |
NM_002613.4 | 889 | Missense Mutation | TCC,TGC | S,C 393 | NP_002604.1 | |
NM_031268.5 | 889 | Missense Mutation | TCC,TGC | S,C 266 | NP_112558.2 | |
XM_011522521.2 | 889 | Missense Mutation | TCC,TGC | S,C 427 | XP_011520823.1 | |
XM_011522523.2 | 889 | Missense Mutation | TCC,TGC | S,C 300 | XP_011520825.1 | |
XM_017023271.1 | 889 | Missense Mutation | TCC,TGC | S,C 427 | XP_016878760.1 | |
XM_017023272.1 | 889 | Missense Mutation | TCC,TGC | S,C 395 | XP_016878761.1 | |
XM_017023273.1 | 889 | Missense Mutation | TCC,TGC | S,C 393 | XP_016878762.1 | |
XM_017023274.1 | 889 | Missense Mutation | TCC,TGC | S,C 366 | XP_016878763.1 | |
XM_017023275.1 | 889 | Missense Mutation | TCC,TGC | S,C 300 | XP_016878764.1 | |
XM_017023276.1 | 889 | Missense Mutation | TCC,TGC | S,C 266 | XP_016878765.1 | |
XM_017023277.1 | 889 | Missense Mutation | TCC,TGC | S,C 177 | XP_016878766.1 |