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ACAATCCTTCTTGGCACTGTTTATC[A/G]ACTGGTGGAGGCCCTGGGCTATGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 607860 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
YY1AP1 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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YY1AP1 - YY1 associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198899.1 | 2658 | Silent Mutation | NP_001185828.1 | |||
NM_001198900.1 | 2658 | Silent Mutation | NP_001185829.1 | |||
NM_001198901.1 | 2658 | Silent Mutation | NP_001185830.1 | |||
NM_001198902.1 | 2658 | Silent Mutation | NP_001185831.1 | |||
NM_001198903.1 | 2658 | Silent Mutation | NP_001185832.1 | |||
NM_001198904.1 | 2658 | Silent Mutation | NP_001185833.1 | |||
NM_001198905.1 | 2658 | Silent Mutation | NP_001185834.1 | |||
NM_001198906.1 | 2658 | UTR 3 | NP_001185835.1 | |||
NM_018253.3 | 2658 | Silent Mutation | NP_060723.2 | |||
NM_139118.2 | 2658 | Silent Mutation | NP_620829.1 | |||
NM_139119.2 | 2658 | Silent Mutation | NP_620830.1 | |||
NM_139121.2 | 2658 | Silent Mutation | NP_620832.1 |