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GCGTCCCTGGAGCGGCCGCCTTCCA[A/G]CGTAAGTGGGGCGTGAATGCGGGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603672 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CBFA2T2 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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CBFA2T2 - CBFA2/RUNX1 translocation partner 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001032999.2 | 233 | Silent Mutation | CAA,CAG | Q,Q 11 | NP_001028171.1 | |
NM_001039709.1 | 233 | Intron | NP_001034798.1 | |||
NM_005093.3 | 233 | Intron | NP_005084.1 | |||
XM_011529101.2 | 233 | Intron | XP_011527403.1 | |||
XM_011529102.2 | 233 | Intron | XP_011527404.1 | |||
XM_011529103.2 | 233 | Intron | XP_011527405.1 | |||
XM_011529107.2 | 233 | Intron | XP_011527409.1 | |||
XM_017028121.1 | 233 | Intron | XP_016883610.1 | |||
XM_017028122.1 | 233 | Silent Mutation | CAA,CAG | Q,Q 11 | XP_016883611.1 | |
XM_017028123.1 | 233 | Intron | XP_016883612.1 | |||
XM_017028124.1 | 233 | Intron | XP_016883613.1 | |||
XM_017028125.1 | 233 | Intron | XP_016883614.1 |