Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGACTTGAGCAGCCCCCGCAGCGGG[C/G]GGGCCGCGTCCGCGTCGGCGCTGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
LMTK3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
LMTK3 - lemur tyrosine kinase 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080434.1 | 4389 | Missense Mutation | CCC,CGC | P,R 1353 | NP_001073903.1 | |
XM_011526411.2 | 4389 | Missense Mutation | CCC,CGC | P,R 1350 | XP_011524713.1 | |
XM_011526412.2 | 4389 | Missense Mutation | CCC,CGC | P,R 1339 | XP_011524714.1 |