Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 163905 | |||||||||||||||||||||||||||||
Literature Links: |
HMGB1 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)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
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EUR - Not Available | |||||
AMR - Not Available |
HMGB1 - high mobility group box 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001313892.1 | 1234 | Missense Mutation | CCT,CTT | P,L 98 | NP_001300821.1 | |
NM_001313893.1 | 1234 | Missense Mutation | CCT,CTT | P,L 98 | NP_001300822.1 | |
NM_002128.5 | 1234 | Missense Mutation | CCT,CTT | P,L 98 | NP_002119.1 |