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CTTTGAATGTCCTCTTCTCATTTTA[G/T]GCTTCATCTGTGTTTCCTTTTGCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 189990 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYB 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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MYB - MYB proto-oncogene, transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130172.1 | Intron | NP_001123644.1 | ||||
NM_001130173.1 | Intron | NP_001123645.1 | ||||
NM_001161656.1 | Intron | NP_001155128.1 | ||||
NM_001161657.1 | Intron | NP_001155129.1 | ||||
NM_001161658.1 | Intron | NP_001155130.1 | ||||
NM_001161659.1 | Intron | NP_001155131.1 | ||||
NM_001161660.1 | Intron | NP_001155132.1 | ||||
NM_005375.3 | Intron | NP_005366.2 |