Product Details

SNP ID
rs139779656
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:99174718 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCCACCAGCCACTGCGAGTACAC[A/G]TTCTCGGACGGGATGAGCGCGGCGG
Phenotype
MIM: 606558
Polymorphism
A/G, 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 2400 Silent Mutation AAC,AAT N705N NP_001269166.1
NM_001282238.1 2400 Silent Mutation AAC,AAT N634N NP_001269167.1
NM_022898.2 2400 Silent Mutation AAC,AAT N635N NP_075049.1
NM_138576.3 2400 Silent Mutation AAC,AAT N706N NP_612808.1

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