Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGGACGGGATGAGCGCGGCGGGCG[A/G]CAGCTCCAGGTCCTTCTCCACCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606558 | ||||||||||||||||||||
Literature Links: |
BCL11B 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 |
BCL11B - B-cell CLL/lymphoma 11B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282237.1 | 2371 | Missense Mutation | CCG,TCG | P,S 696 | NP_001269166.1 | |
NM_001282238.1 | 2371 | Missense Mutation | CCG,TCG | P,S 625 | NP_001269167.1 | |
NM_022898.2 | 2371 | Missense Mutation | CCG,TCG | P,S 626 | NP_075049.1 | |
NM_138576.3 | 2371 | Missense Mutation | CCG,TCG | P,S 697 | NP_612808.1 |