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GGTGCAGCTGGTACTTGTCAGGCTT[A/G]TTCACGTGCAGCACCTCCACATTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600189 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLE1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
TLE1 - transducin like enhancer of split 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303103.1 | 2297 | Silent Mutation | AAC,AAT | N,N 697 | NP_001290032.1 | |
NM_001303104.1 | 2297 | Silent Mutation | AAC,AAT | N,N 672 | NP_001290033.1 | |
NM_005077.4 | 2297 | Silent Mutation | AAC,AAT | N,N 687 | NP_005068.2 | |
XM_005252151.1 | 2297 | Silent Mutation | AAC,AAT | N,N 731 | XP_005252208.1 | |
XM_005252152.1 | 2297 | Silent Mutation | AAC,AAT | N,N 730 | XP_005252209.1 | |
XM_005252153.1 | 2297 | Silent Mutation | AAC,AAT | N,N 721 | XP_005252210.1 | |
XM_005252154.1 | 2297 | Silent Mutation | AAC,AAT | N,N 720 | XP_005252211.1 | |
XM_005252156.2 | 2297 | Silent Mutation | AAC,AAT | N,N 696 | XP_005252213.1 | |
XM_005252162.1 | 2297 | Silent Mutation | AAC,AAT | N,N 647 | XP_005252219.1 | |
XM_005252163.2 | 2297 | Silent Mutation | AAC,AAT | N,N 613 | XP_005252220.1 | |
XM_006717258.1 | 2297 | Silent Mutation | AAC,AAT | N,N 730 | XP_006717321.1 | |
XM_006717259.3 | 2297 | Silent Mutation | AAC,AAT | N,N 675 | XP_006717322.1 | |
XM_006717260.1 | 2297 | Silent Mutation | AAC,AAT | N,N 657 | XP_006717323.1 | |
XM_006717261.2 | 2297 | Silent Mutation | AAC,AAT | N,N 616 | XP_006717324.1 | |
XM_006717262.1 | 2297 | Silent Mutation | AAC,AAT | N,N 686 | XP_006717325.1 | |
XM_006717263.1 | 2297 | Silent Mutation | AAC,AAT | N,N 685 | XP_006717326.1 | |
XM_011518951.2 | 2297 | Silent Mutation | AAC,AAT | N,N 686 | XP_011517253.1 | |
XM_017015064.1 | 2297 | Silent Mutation | AAC,AAT | N,N 696 | XP_016870553.1 | |
XM_017015065.1 | 2297 | Silent Mutation | AAC,AAT | N,N 695 | XP_016870554.1 | |
XM_017015066.1 | 2297 | Silent Mutation | AAC,AAT | N,N 641 | XP_016870555.1 |