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TATTTCCACTTCGGCTATATCCACC[A/G]AAGCTCGATGAAGAAAATGGCCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300553 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BRWD3 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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BRWD3 - bromodomain and WD repeat domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153252.4 | 4835 | Silent Mutation | TTC,TTT | F,F 1524 | NP_694984.4 | |
XM_005262113.3 | 4835 | Silent Mutation | TTC,TTT | F,F 1474 | XP_005262170.1 | |
XM_017029384.1 | 4835 | Silent Mutation | TTC,TTT | F,F 1120 | XP_016884873.1 | |
XM_017029385.1 | 4835 | Intron | XP_016884874.1 |