Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000779575 | SCV000916253 | likely pathogenic | Upshaw-Schulman syndrome | 2018-12-04 | criteria provided, single submitter | clinical testing | The ADAMTS13 c.2017A>T (p.Ile673Phe) missense variant has been reported in a compound heterozygous state in two patients with thrombotic thrombocytopenia purpura who had less than three percent of normal ADAMTS13 enzyme activity in human plasma and in one reportedly healthy individual with low (below 47% of normal) ADAMTS13 enzyme activity, where zygosity information is not provided (Matsumoto et al. 2004; Kokame et al. 2011). This variant was absent from 96 controls and is not reported in the 1000 Genomes Project, the Exome Variant Server, or the Exome Aggregation Consortium. The p.Ile673Phe variant protein was shown to be produced in normal amounts, but expression analysis in HeLa cells demonstrated absent secretion from cells, as is normal for the wild type protein (Matsumoto et al. 2004). Based on the evidence, the p.Ile673Phe variant is classified as likely pathogenic for familial thrombotic thrombocytopenia purpura. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population. |
Uni |
RCV000059761 | SCV000091331 | not provided | not provided | no assertion provided | not provided |