Product Details

SNP ID
rs12890136
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:99175009 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTGTCGGCCAGGAGCTCGCCGTA[A/C]TGCGGCAGTGCGCCTAGGCCCACGT
Phenotype
MIM: 606558
Polymorphism
A/C, Transversion 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 2109 Missense Mutation CAG,CAT Q608H NP_001269166.1
NM_001282238.1 2109 Missense Mutation CAG,CAT Q537H NP_001269167.1
NM_022898.2 2109 Missense Mutation CAG,CAT Q538H NP_075049.1
NM_138576.3 2109 Missense Mutation CAG,CAT Q609H NP_612808.1

View Full Product Details