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CCTGGAAAATGCTGGCCCCGTACGG[C/T]GTCCTCCAGGCGTTGAGCAGGTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601041 MIM: 612399 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLE2 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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TLE2 - transducin like enhancer of split 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144761.1 | 2400 | Intron | NP_001138233.1 | |||
NM_001144762.1 | 2400 | Silent Mutation | ACA,ACG | T,T 578 | NP_001138234.1 | |
NM_001300846.1 | 2400 | Silent Mutation | ACA,ACG | T,T 701 | NP_001287775.1 | |
NM_003260.4 | 2400 | Silent Mutation | ACA,ACG | T,T 700 | NP_003251.2 | |
XM_006722864.2 | 2400 | Intron | XP_006722927.1 | |||
XM_011528230.1 | 2400 | Silent Mutation | ACA,ACG | T,T 689 | XP_011526532.1 |
TLE6 - transducin like enhancer of split 6 | ||||||
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There are no transcripts associated with this gene. |