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CTGGCTCCGGGTGATCTCCAGGGAG[C/T]CACTGACCCCTCTCTGAGCCTGATT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
26 submissions
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Phenotype: |
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Literature Links: |
THEMIS2 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)
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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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THEMIS2 - thymocyte selection associated family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039477.2 | Intron | NP_001034566.1 | ||||
NM_001105556.2 | Intron | NP_001099026.1 | ||||
NM_001286113.1 | Intron | NP_001273042.1 | ||||
NM_001286115.1 | Intron | NP_001273044.1 | ||||
NM_004848.3 | Intron | NP_004839.2 | ||||
XM_005246041.3 | Intron | XP_005246098.1 | ||||
XM_006711050.1 | Intron | XP_006711113.1 | ||||
XM_011542445.2 | Intron | XP_011540747.1 |