BCL11A NC_000002.12:g.60486100A>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution on chromosome 2 at genomic position 60486100 located within intron 2 of the BCL11A gene where adenine has been mutated to guanine.

**Synonyms:** - B Cell CLL/Lymphoma 11A c.386-17267T>C - BAF Chromatin Remodeling Complex Subunit BCL11A c.386-17267T>C - BCL11A - rs10189857 A>G - BCL11A NM_022893.4:c.386-17267T>C - BCL11A c.386-22075G>T - CTIP1 c.386-17267T>C - EVI9 c.386-17267T>C - NC_000002.12:g.60486100A>G - NM_022893.4:c.386-17267T>C - SMARCM1 c.386-17267T>C - ZNF856 c.386-17267T>C