Product Details

SNP ID
rs147218517
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:99175399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGGCCGGCCAGCGAGCCGGCCTT[A/G]TGCATGTGCGTCTTCATGTGGCGCT
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 1719 Silent Mutation NP_001269166.1
NM_001282238.1 1719 Silent Mutation NP_001269167.1
NM_022898.2 1719 Silent Mutation NP_075049.1
NM_138576.3 1719 Silent Mutation NP_612808.1

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