Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001260903 | SCV001430674 | likely pathogenic | Nicolaides-Baraitser syndrome | 2020-08-07 | criteria provided, single submitter | clinical testing | The SMARCA2 variant c.3457-2A>T (p.(?)) is not found in known databases (ExAC or gnomAD). This substitution is located in the acceptor splice site of intron 24. The consequence of this change is not predictable, but a skip of exon 25 is very likely. After the possible exon skipping of exon 25 of the SMARCA2 gene, the sequence remains in-frame, so that this may lead to a milder expression of the disease. The mutation (most likely) leads to a splice defect. The splice site prediction programs predict a change in splicing. ACMG criteria used for classification: PVS1_vstr, PM2. |