Fig. 3: Graphical overview of the JARID2 single-nucleotide variants and deletions.
From: JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome
Location of the single nucleotide variants and deletions (introns not drawn to scale) (a) and conservation of the amino acids affected by missense variants (b). All variants based on NM_004973.4.
