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GAGAAAAGTAATCGAAAGCCAAGCA[C/T]GGCAGACTATCATGGGGGTAGCCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607275 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HOPX 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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HOPX - HOP homeobox | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145459.1 | 812 | Intron | NP_001138931.1 | |||
NM_001145460.1 | 812 | Silent Mutation | CCA,CCG | P,P 94 | NP_001138932.1 | |
NM_032495.5 | 812 | Intron | NP_115884.4 | |||
NM_139211.4 | 812 | Intron | NP_631957.1 | |||
NM_139212.3 | 812 | Intron | NP_631958.1 | |||
XM_006714052.2 | 812 | Silent Mutation | CCA,CCG | P,P 94 | XP_006714115.1 | |
XM_017008728.1 | 812 | Intron | XP_016864217.1 | |||
XM_017008729.1 | 812 | Intron | XP_016864218.1 | |||
XM_017008730.1 | 812 | Intron | XP_016864219.1 | |||
XM_017008731.1 | 812 | Intron | XP_016864220.1 | |||
XM_017008732.1 | 812 | Intron | XP_016864221.1 | |||
XM_017008733.1 | 812 | Intron | XP_016864222.1 | |||
XM_017008734.1 | 812 | Intron | XP_016864223.1 |