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ACATGGTCCCTGTCTCAGCTCCTCC[A/G]GCTCCTGGAAACAAGGGCCCAGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612457 MIM: 602990 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARID3B 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ARID3B - AT-rich interaction domain 3B | ||||||
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There are no transcripts associated with this gene. |
CLK3 - CDC like kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130028.1 | 2570 | Intron | NP_001123500.1 | |||
NM_003992.4 | 2570 | Intron | NP_003983.2 | |||
XM_005254151.3 | 2570 | Intron | XP_005254208.1 | |||
XM_011521205.2 | 2570 | Intron | XP_011519507.1 | |||
XM_011521206.2 | 2570 | Intron | XP_011519508.1 | |||
XM_011521209.2 | 2570 | Intron | XP_011519511.2 | |||
XM_017021905.1 | 2570 | Intron | XP_016877394.1 | |||
XM_017021906.1 | 2570 | Intron | XP_016877395.1 | |||
XM_017021907.1 | 2570 | Intron | XP_016877396.1 | |||
XM_017021908.1 | 2570 | Intron | XP_016877397.1 | |||
XM_017021909.1 | 2570 | Intron | XP_016877398.1 | |||
XM_017021910.1 | 2570 | Intron | XP_016877399.1 |
LOC102723750 - uncharacterized LOC102723750 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017022789.1 | 2570 | Silent Mutation | GCC,GCT | A,A 277 | XP_016878278.1 | |
XM_017022790.1 | 2570 | Silent Mutation | GCC,GCT | A,A 277 | XP_016878279.1 | |
XM_017022791.1 | 2570 | Silent Mutation | GCC,GCT | A,A 277 | XP_016878280.1 | |
XM_017022792.1 | 2570 | Silent Mutation | GCC,GCT | A,A 261 | XP_016878281.1 | |
XM_017022793.1 | 2570 | Intron | XP_016878282.1 | |||
XM_017022794.1 | 2570 | Intron | XP_016878283.1 | |||
XM_017022795.1 | 2570 | Intron | XP_016878284.1 | |||
XM_017022796.1 | 2570 | Silent Mutation | GCC,GCT | A,A 207 | XP_016878285.1 | |
XM_017022797.1 | 2570 | Silent Mutation | GCC,GCT | A,A 207 | XP_016878286.1 | |
XM_017022798.1 | 2570 | Intron | XP_016878287.1 |
Set Membership: |
HapMap |