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TGCCAACCTCCTTCTAGATAGGAAA[C/T]GTCTTACAGATTGTGGAGAGCTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612399 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLE6 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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TLE6 - transducin like enhancer of split 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143986.1 | 262 | Silent Mutation | AAC,AAT | N,N 77 | NP_001137458.1 | |
NM_024760.2 | 262 | UTR 5 | NP_079036.1 | |||
XM_005259645.2 | 262 | Silent Mutation | AAC,AAT | N,N 77 | XP_005259702.1 | |
XM_011528300.2 | 262 | Missense Mutation | AAC,AAT | N,N 77 | XP_011526602.1 | |
XM_011528301.1 | 262 | UTR 5 | XP_011526603.1 | |||
XM_011528306.1 | 262 | UTR 5 | XP_011526608.1 |