Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGGATATTCTCTTTGTCTTCTCTA[C/T]CACCACAGGTTCCATTACAGGAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604727 | ||||||||||||||||||||
Literature Links: |
STK17B 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 |
STK17B - serine/threonine kinase 17b | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004226.3 | 1331 | Missense Mutation | GAT,GGT | D,G 336 | NP_004217.1 | |
XM_011512168.2 | 1331 | Missense Mutation | GAT,GGT | D,G 336 | XP_011510470.1 | |
XM_011512169.1 | 1331 | Missense Mutation | GAT,GGT | D,G 336 | XP_011510471.1 | |
XM_011512170.1 | 1331 | Missense Mutation | GAT,GGT | D,G 336 | XP_011510472.1 | |
XM_011512171.2 | 1331 | Missense Mutation | GAT,GGT | D,G 208 | XP_011510473.1 |