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TATGCGTCTTCAGAAAATACTGACC[G/T]GCGATAATACTTGAGTCTGTGTCTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611416 | |||||||||||||||||||||||
Literature Links: |
TOX3 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
TOX3 - TOX high mobility group box family member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080430.3 | 1962 | Missense Mutation | CAG,CCG | Q,P 572 | NP_001073899.2 | |
NM_001146188.2 | 1962 | Missense Mutation | CAG,CCG | Q,P 567 | NP_001139660.1 | |
XM_005255892.3 | 1962 | Missense Mutation | CAG,CCG | Q,P 571 | XP_005255949.1 | |
XM_011523002.2 | 1962 | Missense Mutation | CAG,CCG | Q,P 549 | XP_011521304.1 | |
XM_017023142.1 | 1962 | Missense Mutation | CAG,CCG | Q,P 568 | XP_016878631.1 |