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AGGATGCTTGTTATTGGGCGAGGTG[A/G]GTGTGTCCCAGGCCTTGGTGCTACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604861 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LATS2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LATS2 - large tumor suppressor kinase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014572.2 | 3554 | Missense Mutation | CCC,CTC | P,L 1025 | NP_055387.2 | |
XM_005266342.1 | 3554 | Missense Mutation | CCC,CTC | P,L 1025 | XP_005266399.1 | |
XM_011535042.2 | 3554 | Missense Mutation | CCC,CTC | P,L 938 | XP_011533344.1 | |
XM_017020541.1 | 3554 | Missense Mutation | CCC,CTC | P,L 918 | XP_016876030.1 | |
XM_017020542.1 | 3554 | UTR 3 | XP_016876031.1 |