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AGTCAATGTCACTGAGGTCGCTGGT[A/C]GGCTCCCCGTGGACGCGGCTCAGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604589 | ||||||||||||||||||||
Literature Links: |
BRD1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
BRD1 - bromodomain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304808.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1181 | NP_001291737.1 | |
NM_001304809.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1050 | NP_001291738.1 | |
XM_011530073.1 | 2621 | Silent Mutation | CCG,CCT | P,P 776 | XP_011528375.1 | |
XM_017028714.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1179 | XP_016884203.1 | |
XM_017028715.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1181 | XP_016884204.1 | |
XM_017028716.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1181 | XP_016884205.1 | |
XM_017028717.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1181 | XP_016884206.1 | |
XM_017028718.1 | 2621 | Silent Mutation | CCG,CCT | P,P 1015 | XP_016884207.1 | |
XM_017028719.1 | 2621 | Intron | XP_016884208.1 | |||
XM_017028720.1 | 2621 | Intron | XP_016884209.1 | |||
XM_017028721.1 | 2621 | Intron | XP_016884210.1 | |||
XM_017028722.1 | 2621 | Silent Mutation | CCG,CCT | P,P 794 | XP_016884211.1 | |
XM_017028723.1 | 2621 | Silent Mutation | CCG,CCT | P,P 635 | XP_016884212.1 |