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CTGTCCTGTTATTTCTCTCGCCGAC[A/G]ATCCCTGGCCACCGGGCTGGCACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608992 MIM: 615765 | ||||||||||||||||||||
Literature Links: |
BCL6B 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 |
BCL6B - B-cell CLL/lymphoma 6B | ||||||
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There are no transcripts associated with this gene. |
SLC16A11 - solute carrier family 16 member 11 | ||||||
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There are no transcripts associated with this gene. |
SLC16A13 - solute carrier family 16 member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_201566.2 | 718 | Missense Mutation | CAA,CGA | Q,R 137 | NP_963860.1 |