Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000707779 | SCV000836889 | pathogenic | Hereditary nonpolyposis colorectal neoplasms | 2021-08-04 | criteria provided, single submitter | clinical testing | This variant is a gross deletion of the genomic region encompassing exon(s) 14-15 of the MSH2 gene. This deletion is out-of-frame, and is expected to create a premature translational stop signal and result in an absent or disrupted protein product. Loss-of-function variants in MSH2 are known to be pathogenic (PMID: 15849733, 24362816). A similar copy number variant has been observed in individual(s) with Lynch syndrome (PMID: 17312306, 18330910). For these reasons, this variant has been classified as Pathogenic. |