Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Victorian Clinical Genetics Services, |
RCV000496973 | SCV005085918 | likely pathogenic | Microcephaly, short stature, and limb abnormalities | 2024-09-20 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as Likely pathogenic. Following criteria are met: 0102 - Loss of function is a known mechanism of disease in this gene and is associated with microcephaly, short stature, and limb abnormalities (MIM#617604) and microcephaly-micromelia syndrome (MIM#251230). (I) 0106 - This gene is associated with autosomal recessive disease. However, there has been one previous report of an individual with femoral facial syndrome who was heterozygous for a single DONSON variant (PMID: 31407851). (I) 0200 - Variant is predicted to result in a missense amino acid change from phenylalanine to leucine. (I) 0251 - This variant is heterozygous. (I) 0304 - Variant is present in gnomAD (v2) <0.01 for a recessive condition (1 heterozygote, 0 homozygotes). (SP) 0501 - Missense variant consistently predicted to be damaging by multiple in silico tools or highly conserved with a major amino acid change. (SP) 0604 - Variant is not located in an established domain, motif, hotspot or informative constraint region. (I) 0705 - No comparable missense variants have previous evidence for pathogenicity. (I) 0803 - This variant has limited previous evidence of pathogenicity in an unrelated individual. This variant was observed as compound heterozygous in an individual with microcephaly and short stature (PMID: 28191891). (SP) 0905 - No published segregation evidence has been identified for this variant. (I) 1002 - This variant has moderate functional evidence supporting abnormal protein function. Cells from a patient compound heterozygous for this variant showed defective intra-S phase checkpoint activation, elevated DNA damage and chromosome breakage, and reduced DONSON protein levels. HeLa cells transfected with this variant showed diffuse protein mislocalisation compared to wild type which was localised in the nucleus (PMID: 28191891). (SP) 1201 - Heterozygous variant detected in trans with a second likely pathogenic heterozygous variant (NM_017613.3:c.670C>T; p.(Pro224Ser)) in a recessive disease. (I) 1205 - This variant has been shown to be maternally inherited (by trio analysis). (I) Legend: (SP) - Supporting pathogenic, (I) - Information, (SB) - Supporting benign |
| OMIM | RCV000496973 | SCV000588194 | pathogenic | Microcephaly, short stature, and limb abnormalities | 2017-08-04 | no assertion criteria provided | literature only |