Product Details

SNP ID
rs61754124
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:99175292 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCGCTCTCGTGGTGGCGGAAGTCA[C/T]CGTCGGCCGCCTTGAGGCCCTCGCC
Phenotype
MIM: 606558
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BCL11B PubMed Links

Gene Details

Gene
BCL11B
Gene Name
B-cell CLL/lymphoma 11B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282237.1 1826 Missense Mutation GAT,GGT D514G NP_001269166.1
NM_001282238.1 1826 Missense Mutation GAT,GGT D443G NP_001269167.1
NM_022898.2 1826 Missense Mutation GAT,GGT D444G NP_075049.1
NM_138576.3 1826 Missense Mutation GAT,GGT D515G NP_612808.1

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