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AGCCTTGACAACTCCCTTTTTTGCT[A/G]CATCAGGCTTTCCTTTAGCTCGATA
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
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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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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 | 1450 | Missense Mutation | NP_001300821.1 | |||
NM_001313893.1 | 1450 | Missense Mutation | NP_001300822.1 | |||
NM_002128.5 | 1450 | Missense Mutation | NP_002119.1 |