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AGCCGGTGGTGTGCTAACTTGGTCC[A/G]CATTACTGGGTGTGACGTGGAGTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605680 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BAZ1A 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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BAZ1A - bromodomain adjacent to zinc finger domain 1A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013448.2 | 3320 | Missense Mutation | GCG,GTG | A,V 1542 | NP_038476.2 | |
NM_182648.1 | 3320 | Missense Mutation | GCG,GTG | A,V 1510 | NP_872589.1 | |
XM_011536374.1 | 3320 | Missense Mutation | GCG,GTG | A,V 1449 | XP_011534676.1 | |
XM_011536376.2 | 3320 | Missense Mutation | GCG,GTG | A,V 1065 | XP_011534678.2 | |
XM_017020942.1 | 3320 | Missense Mutation | GCG,GTG | A,V 1033 | XP_016876431.1 |