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CTAAGAACAAGGTTGTTGCTGAGAC[A/G]AAGGAAGGAGCTCTGTCAGAGCCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300921 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BHLHB9 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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BHLHB9 - basic helix-loop-helix domain containing, class B, 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142524.1 | 845 | Silent Mutation | ACA,ACG | T,T 70 | NP_001135996.1 | |
NM_001142525.1 | 845 | Silent Mutation | ACA,ACG | T,T 70 | NP_001135997.1 | |
NM_001142526.1 | 845 | Intron | NP_001135998.1 | |||
NM_001142527.1 | 845 | Intron | NP_001135999.1 | |||
NM_001142528.1 | 845 | Intron | NP_001136000.1 | |||
NM_001142529.1 | 845 | Intron | NP_001136001.1 | |||
NM_001142530.1 | 845 | Intron | NP_001136002.1 | |||
NM_030639.2 | 845 | Silent Mutation | ACA,ACG | T,T 70 | NP_085142.1 |