Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Clin |
RCV000000329 | SCV005442517 | pathogenic | Von Willebrand disease type 2B | 2024-08-12 | reviewed by expert panel | curation | The NM_000552.5(VWF):c.3940G>C (p.Val1314Leu) missense variant has been reported in at least 3 probands with VWD 2B phenotypes (PS4_moderate; PMIDs: 1419803, 27215777, ISTH 2015 Congress Poster). At least one proband displayed excessive mucocutaneous bleeding as well as a laboratory phenotypes of loss of high molecular weight multimers and an increased response to LD-RIPA showing gain of function, which together are highly specific for VWD type 2B (PP4_moderate; PMID: 1419803). The variant was identified as a de novo occurrence in this patient (PS2_Moderate; PMIDs: 1419803). This variant is absent from gnomAD v4.1 (PM2_Supporting). A Platelet binding assay performed with the Val1314Leu recombinant mutant vWF expressed by COS-7 showed increased binding in the absence of, or at low doses, of ristocetin, indicating that this variant has a gain of function effect on the protein (PMID: 8630394; PS3). In summary, the variant meets the criteria to be classified as Likely Pathogenic for von Willebrand disease type 2B based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD VCEP: PS3, PS4_moderate, PS2_Moderate, PP4_moderate, and PM2_supporting. |
OMIM | RCV000000329 | SCV000020473 | pathogenic | Von Willebrand disease type 2B | 2010-05-01 | no assertion criteria provided | literature only | |
Academic Unit of Haematology, |
RCV000087017 | SCV000118914 | not provided | not provided | no assertion provided | not provided |