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. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Hum Mutat. 2022 May 20;43(9):1149–1161. doi: 10.1002/humu.24398

Figure 2: All DOCK variants identified and sorted in ClinVar.

Figure 2:

Comprehensive analysis at all DOCK variants identified on ClinVar. We sorted variants for their percentage (%) pathogenicity (A), by molecular consequence as either frameshift, nonsense, or missense (B) and sorted by variant type, as either deletion, duplication, indel, insertion, or single nucleotide (C).