Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Victorian Clinical Genetics Services, |
RCV002471882 | SCV002767492 | uncertain significance | Orofacial cleft 11 | 2022-03-31 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as VUS-3B. Following criteria are met: 0102 - Loss of function is a known mechanism of disease in this gene and is associated with microphthalmia, syndromic 6 (MIM#607932) and orofacial cleft 11 (MIM#600625) (PMIDs: 21340693, 30568244). (I) 0107 - This gene is associated with autosomal dominant disease. (I) 0112 - The condition associated with this gene has incomplete penetrance. Affected children have been found to carry the same BMP4 variant as their unaffected parent (PMIDs: 31053785, 19249007, 21340693). (I) 0115 - Variants in this gene are known to have variable expressivity. Individuals with orofacial clefts or microphthalmia have been found to carry the same BMP4 variants as their mildly affected parents (PMID: 19249007, 21340693). (I) 0200 - Variant is predicted to result in a missense amino acid change from phenylalanine to leucine. (I) 0219 - This variant is non-coding in an alternative transcript. However, this variant is coding in the ClinVar predominant and MANE select transcript (NM_001202). (I) 0251 - This variant is heterozygous. (I) 0302 - Variant is present in gnomAD (v2) <0.001 for a dominant condition (1 heterozygote, 0 homozygotes). (SP) 0503 - Missense variant consistently predicted to be tolerated by multiple in silico tools or highly in placental mammals with a minor amino acid change. (SB) 0600 - Variant is located in the annotated TGF-beta propeptide domain (DECIPHER). (I) 0705 - No comparable missense variants have previous evidence for pathogenicity. (I) 0807 - This variant has no previous evidence of pathogenicity. (I) 0905 - No published segregation evidence has been identified for this variant. (I) 1007 - No published functional evidence has been identified for this variant. (I) 1208 - Inheritance information for this variant is not currently available in this individual. (I) Legend: (SP) - Supporting pathogenic, (I) - Information, (SB) - Supporting benign |