Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605132 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLE4 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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TLE4 - transducin like enhancer of split 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282748.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | NP_001269677.1 | |
NM_001282749.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | NP_001269678.1 | |
NM_001282753.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | NP_001269682.1 | |
NM_001282760.1 | 236 | UTR 5 | NP_001269689.1 | |||
NM_007005.4 | 236 | Silent Mutation | CCA,CCG | P,P 15 | NP_008936.2 | |
XM_005252177.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_005252234.1 | |
XM_006717264.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_006717327.1 | |
XM_006717268.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_006717331.1 | |
XM_011518952.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517254.1 | |
XM_011518953.1 | 236 | Intron | XP_011517255.1 | |||
XM_011518954.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517256.1 | |
XM_011518955.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517257.1 | |
XM_011518956.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517258.1 | |
XM_011518957.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517259.1 | |
XM_011518958.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517260.1 | |
XM_011518959.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517261.1 | |
XM_011518960.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517262.1 | |
XM_011518961.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517263.1 | |
XM_011518962.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517264.1 | |
XM_011518963.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517265.1 | |
XM_011518964.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517266.1 | |
XM_011518965.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517267.1 | |
XM_011518966.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517268.1 | |
XM_011518967.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517269.1 | |
XM_011518968.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517270.1 | |
XM_011518969.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517271.1 | |
XM_011518970.2 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_011517272.1 | |
XM_011518972.2 | 236 | Intron | XP_011517274.1 | |||
XM_017015067.1 | 236 | Intron | XP_016870556.1 | |||
XM_017015068.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870557.1 | |
XM_017015069.1 | 236 | Intron | XP_016870558.1 | |||
XM_017015070.1 | 236 | Intron | XP_016870559.1 | |||
XM_017015071.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870560.1 | |
XM_017015072.1 | 236 | Intron | XP_016870561.1 | |||
XM_017015073.1 | 236 | Intron | XP_016870562.1 | |||
XM_017015074.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870563.1 | |
XM_017015075.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870564.1 | |
XM_017015076.1 | 236 | Intron | XP_016870565.1 | |||
XM_017015077.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870566.1 | |
XM_017015078.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870567.1 | |
XM_017015079.1 | 236 | Intron | XP_016870568.1 | |||
XM_017015080.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870569.1 | |
XM_017015081.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870570.1 | |
XM_017015082.1 | 236 | Intron | XP_016870571.1 | |||
XM_017015083.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870572.1 | |
XM_017015084.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870573.1 | |
XM_017015085.1 | 236 | Intron | XP_016870574.1 | |||
XM_017015086.1 | 236 | Silent Mutation | CCA,CCG | P,P 15 | XP_016870575.1 |