BCL11A NC_000002.12:g.60490908=

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution on chromosome 2 at genomic position 60490908 located within intron 2 of the BCL11A gene where thymine is present instead of guanine.

**Synonyms:** - B Cell CLL/Lymphoma 11A c.386-22075= - BAF Chromatin Remodeling Complex Subunit BCL11A c.386-22075= - BCL11A - rs1427407 G>T - BCL11A NM_022893.4:c.386-22075= - BCL11A c.386-22075= - BCL11A c.386-22075G>T - CTIP1 c.386-22075= - EVI9 c.386-22075= - NG_011968.1:g.67591= - NM_022893.4:c.386-22075= - SMARCM1 c.386-22075= - ZNF856 c.386-22075=