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TCTTACGGCAAGGTGAAGGAGGTGC[C/T]GGACTCGGAGACGCTGTGCAGGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602216 | ||||||||||||||||||||
Literature Links: |
STK11 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 |
STK11 - serine/threonine kinase 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000455.4 | 825 | Missense Mutation | CCG,CTG | P,L 67 | NP_000446.1 | |
XM_005259617.2 | 825 | Missense Mutation | CCG,CTG | P,L 67 | XP_005259674.1 | |
XM_005259618.3 | 825 | Missense Mutation | CCG,CTG | P,L 67 | XP_005259675.1 | |
XM_011528209.1 | 825 | UTR 5 | XP_011526511.1 |